Medizinisches Versorgungszentrum DRK Blutspendedienst Frankfurt gemeinnützige
Official name: Medizinisches Versorgungszentrum DRK Blutspendedienst Frankfurt gemeinnützige GmbH
202 capabilities
Accredited since February 2026
Verified Apr 2026
One of 3,039 in Germany
Details
Sandhofstraße 1
Frankfurt/Main 60528 , Germany
Frankfurt/Main 60528 , Germany
Accreditation
Active
DAkkS
D-ML-13315-01-01
Transfusion medicine and clinical laboratory providing testing across clinical chemistry, immunology, human genetics, and transfusion medicine. Includes flow cytometric cell enumeration and particle counting on blood samples, alongside ligand assays via ELISA.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-13315-01-01
Status
ActiveSince
27 February 2026
Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.
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Test Capabilities (202)
| Standard Reference | Description | Category |
|---|---|---|
| AB0 System | AB0-System | Biocompatibility (ISO 10993) |
| Antikörper Screening | Antikörper-Screening | Biocompatibility (ISO 10993) |
| Arrhythmogene rechtsventrikuläre | Arrhythmogene rechtsventrikuläre | Biocompatibility (ISO 10993) |
| HLA Klasse II | HLA-Klasse II | Biocompatibility (ISO 10993) |
| HLA-Antikörper Screening | HLA-Antikörper Screening | Biocompatibility (ISO 10993) |
| Verträglichkeitsprobe | serol. Verträglichkeitsprobe | Biocompatibility (ISO 10993) |
| RHCE | RHD und RHCE | Biological / Microbiological |
| (HBG1 und HBG2 ) | (HBG1 und HBG2 ) | Chromatography (GC, HPLC) |
| ACKR1 (Duffy-Blutgruppe) | ACKR1 (Duffy-Blutgruppe) | Chromatography (GC, HPLC) |
| Blutgruppe) | RHD, RHCE (Rh-Blutgruppe) | Chromatography (GC, HPLC) |
| Blutgruppen-Polymorphismen | Blutgruppen-Polymorphismen | Chromatography (GC, HPLC) |
| CD109 (HPA-15) | CD109 (HPA-15) | Chromatography (GC, HPLC) |
| FUT2 (Lewis-Blutgruppe) | FUT2 (Lewis-Blutgruppe) | Chromatography (GC, HPLC) |
| FUT3 (Lewis-Blutgruppe) | FUT3 (Lewis-Blutgruppe) | Chromatography (GC, HPLC) |
| GYPA, GYPB (MNS-Blutgruppe) | GYPA, GYPB (MNS-Blutgruppe) | Chromatography (GC, HPLC) |
| HJV , HAMP , TFR2 , SLC11A3 | HJV , HAMP , TFR2 , SLC11A3 | Chromatography (GC, HPLC) |
| Hereditäre Persistenz von | Hereditäre Persistenz von | Chromatography (GC, HPLC) |
| KEL (Kell-Blutgruppe) | KEL (Kell-Blutgruppe) | Chromatography (GC, HPLC) |
| SLC14A1 (Kidd-Blutgruppe) | SLC14A1 (Kidd-Blutgruppe) | Chromatography (GC, HPLC) |
| XK (Kx-Blutgruppe) | XK (Kx-Blutgruppe) | Chromatography (GC, HPLC) |
| morphismen (HPA-1, -2, 9 -15) (SSP-PCR) | morphismen (HPA-1, -2, 9 -15) (SSP-PCR) | Chromatography (GC, HPLC) |
| sonstige Hämoglobinopahtien | sonstige Hämoglobinopahtien | Chromatography (GC, HPLC) |
| (VWF:Ac) | (VWF:CB) | Clinical Chemistry |
| Blutgruppenallele | Blutgruppenallele | Elemental Analysis |
| Catecholaminerge polymorphe | Catecholaminerge polymorphe | Elemental Analysis |
| Hämatokrit | Hämatokrit | Elemental Analysis |
| MCV | MCV | Elemental Analysis |
| Erythrozytä re Antigene | Erythrozytäre Antigene | Food Safety Testing |
| Kell-Merkmal K | Kell-Merkmal K | Food Safety Testing |
| Rh-Untergruppen | Rh-Untergruppen | Food Safety Testing |
| IRHD N 30 IRHD | IRHD N 30 IRHD | Hardness (Vickers, Rockwell, Brinell) |
| - Basophile | Basophile | Hematology |
| - Eosinophile | Eosinophile | Hematology |
| - Erythrozyten | Erythrozyten | Hematology |
| - Leukozyten | Leukozyten | Hematology |
| - Lymphozyten | Lymphozyten | Hematology |
| - Monozyten | Monozyten | Hematology |
| - Thrombozyten | Thrombozyten | Hematology |
| Coombs-Test | Direkter Coombstest | Hematology |
| Coombstest | polyspezifischer direkter Coombstest | Hematology |
| Kreuzprobe | Kreuzprobe | Hematology |
| Neutrophile Granulozyten | Neutrophile Granulozyten | Hematology |
| (DAT bzw. DCT) | (DAT bzw. DCT) | Immunology / Serology |
| AB0 | Blutgruppe AB0 | Immunology / Serology |
| AB0-Blutgruppe und RhD | AB0-Blutgruppe und RhD | Immunology / Serology |
| Antigen D im indirekten | Antigen-D im indirekten | Immunology / Serology |
| Antihumanglobulintest | Direkter Antihumanglobulintest | Immunology / Serology |
| Antikörper Differenzierung | Antikörperdifferenzierung | Immunology / Serology |
| Antikörper Titer | Hepatitis-B-Antikörper Titer | Immunology / Serology |
| Antikörpernachweis, Kreuzprobe | Antikörpernachweis, Kreuzprobe | Immunology / Serology |
| Antikörperscreening | Hepatitis C-Antikörper-Screening | Immunology / Serology |
| Gebundene Antikörper | Gebundene Antikörper | Immunology / Serology |
| HLA Klasse I (A/B/C) | HLA Klasse I (A/B/C) | Immunology / Serology |
| HLA-Antikörper Differenzierung | HLA-Antikörperdifferenzierung | Immunology / Serology |
| Kreuzprobe/Serologische | Kreuzprobe/Serologische | Immunology / Serology |
| Lymphozyten CD34+ | Lymphozyten CD34+ | Immunology / Serology |
| Rh-Merkmal D | Rh-Merkmal D | Immunology / Serology |
| Rhesus-Formel und Kell-Antigen | Rhesusformel und Kell-Antigen | Immunology / Serology |
| Verträglichkeitsprobe im | Verträglichkeitsprobe im | Immunology / Serology |
| (ADAMTS13 ) | (ADAMTS13) | Molecular Diagnostics / PCR |
| (DSP, LMNA, SCN5A ) | (DSP, LMNA, SCN5A ) | Molecular Diagnostics / PCR |
| (FGA, FGB, FGG) | Afibrinogenämie (FGA, FGB, FGG) | Molecular Diagnostics / PCR |
| (HBB) | Beta-Thalassämie (HBB) | Molecular Diagnostics / PCR |
| (ITGA2B, ITGB3) | (ITGA2B, ITGB3) | Molecular Diagnostics / PCR |
| (MYH7, CASQ2, MYBPC3, TNNT2 ) | (MYH7, CASQ2, MYBPC3, TNNT2 ) | Molecular Diagnostics / PCR |
| (MYH7, CASQ2, MYBPC3, TNNT2, DSP, LMNA ) | (MYH7, CASQ2, MYBPC3, TNNT2, DSP, LMNA ) | Molecular Diagnostics / PCR |
| (MYH7, MYBPC3, TNNT2, FLNC, TTR ) | (MYH7, MYBPC3, TNNT2, FLNC, TTR ) | Molecular Diagnostics / PCR |
| (SSP-PCR) | (SSP-PCR) | Molecular Diagnostics / PCR |
| (TNNI3, MYH7, MYBPC3, FLNC ) | (TNNI3, MYH7, MYBPC3, FLNC ) | Molecular Diagnostics / PCR |
| Andersen-Tawil-Syndrom | Andersen-Tawil-Syndrom | Molecular Diagnostics / PCR |
| Angiödem (F12 ) | Angiödem (F12 ) | Molecular Diagnostics / PCR |
| Antikörper-Differenzierung | erythrozytäre Blutgruppenantigene, Antikörperdifferenzierung | Molecular Diagnostics / PCR |
| Arrhythmogene Kardiomyopathie | Arrhythmogene Kardiomyopathie | Molecular Diagnostics / PCR |
| Autoimmunthrombozytopenie | Autoimmunthrombozytopenie | Molecular Diagnostics / PCR |
| Bindung | Thrombozyten, PAC-1 Bindung | Molecular Diagnostics / PCR |
| Brugada-Syndrom (SCN5A) | Brugada-Syndrom (SCN5A) | Molecular Diagnostics / PCR |
| Cardiac Conduction Disease | Cardiac Conduction Disease | Molecular Diagnostics / PCR |
| Compaction-Kardiomyopathie | Non-compaction Kardiomyopathie | Molecular Diagnostics / PCR |
| Dilatative Kardiomyopathie | Dilatative Kardiomyopathie | Molecular Diagnostics / PCR |
| Dissektionen (LOX, PRKG1) | Dissektionen (LOX, PRKG1) | Molecular Diagnostics / PCR |
| F13B) | Faktor XIII B-Mangel (F13B) | Molecular Diagnostics / PCR |
| HLA-A-Locus | HLA-A-Locus | Molecular Diagnostics / PCR |
| HLA-B-Locus | HLA-B-Locus | Molecular Diagnostics / PCR |
| HLA-C-Locus | HLA-C-Locus | Molecular Diagnostics / PCR |
| HLA-DPA1-Locus | HLA-DPA1-Locus | Molecular Diagnostics / PCR |
| HLA-DPB1 Locus | HLA-DPB1-Locus | Molecular Diagnostics / PCR |
| HLA-DQA1 | HLA-DQA1 | Molecular Diagnostics / PCR |
| HLA-DQA1-Locus | HLA-DQA1-Locus | Molecular Diagnostics / PCR |
| HLA-DQB1-Locus | HLA-DQB1-Locus | Molecular Diagnostics / PCR |
| HLA-DRB1 -Locus | HLA-DRB1-Locus | Molecular Diagnostics / PCR |
| HLA-DRB3/4/5-Locus | HLA-DRB3/4/5-Locus | Molecular Diagnostics / PCR |
| Hereditäre Hämochromatose | Hereditäre Hämochromatose | Molecular Diagnostics / PCR |
| Hypertrophe Kardiomyopathie | Hypertrophe Kardiomyopathie | Molecular Diagnostics / PCR |
| Infantile und neonatale | Infantile und neonatale | Molecular Diagnostics / PCR |
| KCNE1, KCNE2, KCNJ2, KCNQ1 | KCNE1, KCNE2, KCNJ2, KCNQ1 | Molecular Diagnostics / PCR |
| Kardiomyopathie (PKP2, DSG2, SCN5A ) | Kardiomyopathie (PKP2, DSG2, SCN5A ) | Molecular Diagnostics / PCR |
| Long-QT-Syndrom (KCNQ1, SCN5A, KCNE1, KCNJ2, CACNA1C, CALM2, CALM3) | Long-QT-Syndrom (KCNQ1, SCN5A, KCNE1, KCNJ2, CACNA1C, CALM2, CALM3) | Molecular Diagnostics / PCR |
| MYLK, TGFBR1, TGFBR2 | MYLK, TGFBR1, TGFBR2 | Molecular Diagnostics / PCR |
| Mangel/Dysplasminogenämie | Mangel/Dysplasminogenämie | Molecular Diagnostics / PCR |
| Plasminogen-Mangel/ | Plasminogen-Mangel/ | Molecular Diagnostics / PCR |
| RYR2, CASQ2, KCNJ2, TRDN | RYR2, CASQ2, KCNJ2, TRDN | Molecular Diagnostics / PCR |
| Restriktive Kardiomyopathie | Restriktive Kardiomyopathie | Molecular Diagnostics / PCR |
| Short-QT-Syndrom (KCNH2, KCNQ1) | Short-QT-Syndrom (KCNH2, KCNQ1) | Molecular Diagnostics / PCR |
| TCAP, TNNC1, TPM1, GLA | TCAP, TNNC1, TPM1, GLA | Molecular Diagnostics / PCR |
| Thorakale Aortenaneurysmen | Thorakale Aortenaneurysmen | Molecular Diagnostics / PCR |
| TruSight Cardio Panel, KCNH2, KCNJ2, KCNQ1 | TruSight Cardio Panel, KCNH2, KCNJ2, KCNQ1 | Molecular Diagnostics / PCR |
| Ventrikuläre Tachykardie | ventrikuläre Tachykardie | Molecular Diagnostics / PCR |
| Weitere Blutgruppensysteme | Weitere Blutgruppensysteme | Molecular Diagnostics / PCR |
| dbSNP rs1799889 | dbSNP rs1799889 | Molecular Diagnostics / PCR |
| rs1801133, dbSNP rs1801131 | rs1801133, dbSNP rs1801131 | Molecular Diagnostics / PCR |
| sonstige Hämoglobinopathien | sonstige Hämoglobinopathien | Molecular Diagnostics / PCR |
| weight kininogen deficiency | weight kininogen deficiency | Molecular Diagnostics / PCR |
| (DRB1/DQA1/DQB1/DPA1/ | (DRB1/DQA1/DQB1/DPA1/ | Other |
| (DSP, LMNA, SCN5A, FLNC | (DSP, LMNA, SCN5A, FLNC | Other |
| (F5-Gen: dbSNP | Thrombophilie (F5-Gen: | Other |
| (Illumina TruSight Cardio | (Illumina TruSight Cardio | Other |
| 6), ITGA2B (HPA-3/-9), GP1BA | 6), ITGA2B (HPA-3/-9), GP1BA | Other |
| Alpha-Thalassämie (HBA1 | Alpha-Thalassämie (HBA1 | Other |
| Antithrombin-Mangel (SERPINC1 | Antithrombin-Mangel (SERPINC1 | Other |
| Aspirin-Resistenz (COX1 | Aspirin-Resistenz (COX1 | Other |
| Aspirin-Resistenz (COX1= | Aspirin-Resistenz (COX1= | Other |
| Brugada-Syndrom (Illumina | Brugada-Syndrom (Illumina | Other |
| CACNA1C, CACNB2, SCN1B, KCNE3 ) | CACNA1C, CACNB2, SCN1B, KCNE3 ) | Other |
| CACNA1C, CACNB2, SCN1B, KCNE3, HCN4, TRPM4 ) | CACNA1C, CACNB2, SCN1B, KCNE3, HCN4, TRPM4 ) | Other |
| CACNA2D1, CACNB2, KCNH2, KCNJ2, KCNQ1) | TruSight Cardio Panel, CACNA1C, CACNA2D1, CACNB2, KCNH2, KCNJ2, KCNQ1 ) | Other |
| CASQ2, KCNJ2, CALM2, CALM3, TECRL ) | CASQ2, KCNJ2, CALM2, CALM3, TECRL ) | Other |
| CYP2C9 ) | CYP2C9 ) | Other |
| Cardio Panel, FBN1, TGFBR1, TGFBR2 ) | Cardio Panel, FBN1, TGFBR1, TGFBR2 ) | Other |
| Cardio Panel, GLA ) | Cardio Panel, GLA ) | Other |
| Cardio Panel, PKP2, DSC2, DSG2, JUP, SCN5A ) | Cardio Panel, PKP2, DSC2, DSG2, JUP, SCN5A ) | Other |
| Cardio Panel, SCN5A) | Cardio Panel, SCN5A) | Other |
| Crossmatch | System) inklusive Auto-Crossmatch | Other |
| Crossmatch (serologische | Crossmatch (serologische | Other |
| Cumarin-Resistenz (VKORC1 | Cumarin-Resistenz (VKORC1 | Other |
| Cumarin-Sensitivität (CYP2C9 | Cumarin-Sensitivität (CYP2C9 | Other |
| DPB1/DRB3/DRB4/DRB5) | DPB1/DRB3/DRB4/DRB5) | Other |
| DSG2 ); MLPA: PKP2, DSG2, JUP, DSP, TGFß3, RYR2 | DSG2 ); MLPA: PKP2, DSG2, JUP, DSP, TGFß3, RYR2 | Other |
| DSP, FLNC, JPH2, NEXN, TNNC1, VCL) | DSP, FLNC, JPH2, NEXN, TNNC1, VCL) | Other |
| DSP, FLNC, LMNA, PLN, DES, SCN5A, TMEM43 ) | DSP, FLNC, LMNA, PLN, DES, SCN5A, TMEM43 ) | Other |
| DSP, LMNA, PLN, RBM20, SCN5A, TMEM43 ) | DSP, LMNA, PLN, RBM20, SCN5A, TMEM43 ) | Other |
| Dissektionen (Illumina TruSight | Dissektionen (Illumina TruSight | Other |
| Duffy, Kidd, MNS) und seltene | Duffy, Kidd, MNS) und seltene | Other |
| Dysplasminogenämie (PLG | Dysplasminogenämie (PLG | Other |
| F13B); dbSNP rs5985 | F13B); dbSNP rs5985 | Other |
| Faktor-V-Mangel (F5 inklusive | Faktor-V-Mangel (F5 inklusive | Other |
| Faktor-XIII-Mangel (F13A1 | Faktor-XIII-Mangel (F13A1 | Other |
| GP1BB, GP9 , GP5 ) | GP1BB, GP9 , GP5 ) | Other |
| Homocysteinurie (CBS und | Homocysteinurie (CBS und | Other |
| Kardiomyopathie (Illumina | Kardiomyopathie (Illumina | Other |
| LMNA, MYH7, MYBPC3, TNNI3, SCN5A, BAG3, RBM20, TPM1, TTN ) | LMNA, MYH7, MYBPC3, TNNI3, SCN5A, BAG3, RBM20, TPM1, TTN ) | Other |
| LMNA, SCN5A, TRPM4 ) | LMNA, SCN5A, TRPM4 ) | Other |
| Loeys-Dietz-Syndrom (Illumina | Loeys-Dietz-Syndrom (Illumina | Other |
| Long-QT-Syndrom (CLCN1 | Long-QT-Syndrom (CLCN1 | Other |
| Long-QT-Syndrom (Illumina | Long-QT-Syndrom (Illumina | Other |
| MTHFR ); MTHFR-Gen: dbSNP | MTHFR ); MTHFR-Gen: dbSNP | Other |
| MYH7, MYBPC3, TNNT2, SCN5A ) | MYH7, MYBPC3, TNNT2, SCN5A ) | Other |
| MYH7, MYBPC3, TNNT2, SCN5A, DSP, FLNC ) | MYH7, MYBPC3, TNNT2, SCN5A, DSP, FLNC ) | Other |
| Mangel (GGCX und VKORC1 | Mangel (GGCX und VKORC1 | Other |
| Marfan-Syndrom (Illumina | Marfan-Syndrom (Illumina | Other |
| Morbus Fabry (Illumina | Morbus Fabry (Illumina | Other |
| Morbus Glanzmann (ITGA2B | Morbus Glanzmann (ITGA2B | Other |
| PAI1-Mangel (PAI1= SERPINE1 | PAI1-Mangel (PAI1= SERPINE1 | Other |
| Protein-C-Mangel (PROC | Protein-C-Mangel (PROC | Other |
| Protein-S-Mangel (PROS1 | Protein-S-Mangel (PROS1 | Other |
| Protein-Z-Mangel (PROZ | Protein-Z-Mangel (PROZ | Other |
| Präkallikrein-Mangel (KLKB1 | Präkallikrein-Mangel (KLKB1 | Other |
| RHAG | RHAG | Other |
| Short-QT-Syndrom (Illumina | Short-QT-Syndrom (Illumina | Other |
| Sichelzellkrankheit (HBS | Sichelzellkrankheit (HBS | Other |
| TAZ, TPM1, CASQ2, LDB3, TNNI3, TNNT2 ) | TAZ, TPM1, CASQ2, LDB3, TNNI3, TNNT2 ) | Other |
| TCAP, TNNC1, TPM1, GLA, FXN LAMP2, SCL25A4, TTR) | TCAP, TNNC1, TPM1, GLA, FXN LAMP2, SCL25A4, TTR) | Other |
| TNNI3, DES, MYH7, MYBPC3, TNNT2 ) | TNNI3, DES, MYH7, MYBPC3, TNNT2 ) | Other |
| TNNI3, TNNT2, DSP, LMNA, RBM20, TBX20, TTN ) | TNNI3, TNNT2, DSP, LMNA, RBM20, TBX20, TTN ) | Other |
| TNNT2, ACTC1, FHL1, FLNC, MYL2, TPM1, TTR ) | TNNT2, ACTC1, FHL1, FLNC, MYL2, TPM1, TTR ) | Other |
| TruSight Cardio Panel, CALM1, CALM2, CALM3, RYR2, CASQ2, KCNJ2, TRDN, TECRL ) | TruSight Cardio Panel, CALM1, CALM2, CALM3, RYR2, CASQ2, KCNJ2, TRDN, TECRL ) | Other |
| VIII-Mangel (LMAN1 und | VIII-Mangel (LMAN1 und | Other |
| VKORC1 und CYP4F2 ) | VKORC1 und CYP4F2 ) | Other |
| dbSNP r6027 ) | dbSNP r6027 ) | Other |
| rs6025, F2-Gen: dbSNP rs1799963 | rs6025, F2-Gen: rs1799963) | Other |
| (CO2) | (CO2) | Spectroscopy (XRF, ICP, AAS) |
| A-, Dys-, Hypofibrinogenämie | A-, Dys-, Hypofibrinogenämie | Spectroscopy (XRF, ICP, AAS) |
| Bernard-Soulier-Syndrom | Bernard-Soulier-Syndrom | Spectroscopy (XRF, ICP, AAS) |
| Fa ktor-VII-Mangel (F7 ) | Faktor-VII-Mangel (F7 ) | Spectroscopy (XRF, ICP, AAS) |
| Faktor-X-Mangel (F10 ) | Faktor-X-Mangel (F10 ) | Spectroscopy (XRF, ICP, AAS) |
| Faktor-XI-Mangel (F11 ) | Faktor-XI-Mangel (F11 ) | Spectroscopy (XRF, ICP, AAS) |
| Faktor-XII-Mangel und hereditäres | Faktor-XII-Mangel und hereditäres | Spectroscopy (XRF, ICP, AAS) |
| HLA-Klasse II (DR/DQ/DP) | HLA-Klasse II (DR/DQ/DP) | Spectroscopy (XRF, ICP, AAS) |
| Hereditäre Thrombozytopenie | Hereditäre Thrombozytopenie | Spectroscopy (XRF, ICP, AAS) |
| Hypo-, Dysthrombinämie | Hypo-, Dysthrombinämie | Spectroscopy (XRF, ICP, AAS) |
| Hämoglobin | Hämoglobin | Spectroscopy (XRF, ICP, AAS) |
| Hämophilie A (F8 ) | Hämophilie A (F8 ) | Spectroscopy (XRF, ICP, AAS) |
| Hämophilie B (F9 ) | Hämophilie B(F9 ) | Spectroscopy (XRF, ICP, AAS) |
| Kininogen-Mangel, High | Kininogen-Mangel, High | Spectroscopy (XRF, ICP, AAS) |
| Kombinierter Faktor-V und | Kombinierter Faktor-V und | Spectroscopy (XRF, ICP, AAS) |
| Lymphozyten CD34+/ CD4/ | Lymphozyten CD34+/ CD4/ | Spectroscopy (XRF, ICP, AAS) |
| PAI1-Mangel (PAI1 ) | PAI1-Mangel (PAI1 ) | Spectroscopy (XRF, ICP, AAS) |
| Plasminogen | Plasminogen | Spectroscopy (XRF, ICP, AAS) |
| Protein-C-Rezeptor-Mangel | Protein-C-Rezeptor-Mangel | Spectroscopy (XRF, ICP, AAS) |
| Quebec platelet disorder | Quebec platelet disorder | Spectroscopy (XRF, ICP, AAS) |
| TAFI-Mangel (CPB2 ) | TAFI-Mangel (CPB2 ) | Spectroscopy (XRF, ICP, AAS) |
| VWF-Multimere | vWF-Multimere | Temperature / Pressure |
| 2) | DIN EN 1555-5 | Tensile / Compression / Flexural |