ScopeMedizinisches Versorgungszentrum DRK Blutspendedienst Frankfurt gemeinnützige
Official name: Medizinisches Versorgungszentrum DRK Blutspendedienst Frankfurt gemeinnützige GmbH
184 capabilities
Accredited since February 2026
Verified Sep 2026
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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.
Download Scope PDFAdditional scope documents
Test Capabilities (184)
| 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-Antikörper Screening | HLA-Antikörper Screening | Biocompatibility (ISO 10993) |
| HLA-Klasse II | HLA-Klasse II | Biocompatibility (ISO 10993) |
| monospezifischer Coombstest | monospezifischer Coombstest | Biocompatibility (ISO 10993) |
| serol. Verträglichkeitsprobe | serol. Verträglichkeitsprobe | Biocompatibility (ISO 10993) |
| RHD und RHCE | RHD und RHCE | Biological / Microbiological |
| (HBG1 und HBG2 ) | (HBG1 und HBG2 ) | Chromatography (GC, HPLC) |
| ACKR1 (Duffy-Blutgruppe) | ACKR1 (Duffy-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) |
| RHD, RHCE (Rh-Blutgruppe) | RHD, RHCE (Rh-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:CB) | (VWF:CB) | Clinical Chemistry |
| Collagenbindung | Collagenbindung | Clinical Chemistry |
| Blutgruppenallele | Blutgruppenallele | Elemental Analysis |
| Catecholaminerge polymorphe | Catecholaminerge polymorphe | Elemental Analysis |
| Hämatokrit | Hämatokrit | Elemental Analysis |
| MCV | MCV | Elemental Analysis |
| Erythrozytäre 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 |
| Coombstest | Plasma | Direct Coombs Test | Hematology |
| Direkter Coombstest | Direkter Coombstest | Hematology |
| Eosinophile | Eosinophile | Hematology |
| Erythrozyten | Erythrozyten | Hematology |
| Kreuzprobe | Kreuzprobe | Hematology |
| Leukozyten | Leukozyten | Hematology |
| Lymphozyten | Lymphozyten | Hematology |
| Monozyten | Monozyten | Hematology |
| Neutrophile Granulozyten | Neutrophile Granulozyten | Hematology |
| Thrombozyten | Thrombozyten | Hematology |
| polyspezifischer direkter Coombstest | polyspezifischer direkter Coombstest | Hematology |
| (DAT bzw. DCT) | (DAT bzw. DCT) | Immunology / Serology |
| AB0-Blutgruppe und RhD | AB0-Blutgruppe und RhD | Immunology / Serology |
| Antigen-D im indirekten | Antigen-D im indirekten | Immunology / Serology |
| Antikörperdifferenzierung | Antikörperdifferenzierung | Immunology / Serology |
| Antikörpernachweis, Kreuzprobe | Antikörpernachweis, Kreuzprobe | Immunology / Serology |
| Blutgruppe AB0 | Blutgruppe AB0 | Immunology / Serology |
| Direkter Antihumanglobulintest | Direkter Antihumanglobulintest | Immunology / Serology |
| Gebundene Antikörper | Gebundene Antikörper | Immunology / Serology |
| HLA Klasse I (A/B/C) | HLA Klasse I (A/B/C) | Immunology / Serology |
| HLA-Antikörperdifferenzierung | HLA-Antikörperdifferenzierung | Immunology / Serology |
| Hepatitis C-Antikörper-Screening | Hepatitis C-Antikörper-Screening | Immunology / Serology |
| Hepatitis-B-Antikörper Titer | Hepatitis-B-Antikörper Titer | Immunology / Serology |
| Kreuzprobe/Serologische | Kreuzprobe/Serologische | Immunology / Serology |
| Lymphozyten CD34+ | Lymphozyten CD34+ | Immunology / Serology |
| Rh-Merkmal D | Rh-Merkmal D | Immunology / Serology |
| Rhesusformel und Kell-Antigen | Rhesusformel und Kell-Antigen | Immunology / Serology |
| Verträglichkeitsprobe im | Verträglichkeitsprobe im | Immunology / Serology |
| (ADAMTS13) | (ADAMTS13) | Molecular Diagnostics / PCR |
| (DRB1/DQA1/DQB1/DPA1/ DPB1/DRB3/DRB4/DRB5) | (DRB1/DQA1/DQB1/DPA1/ DPB1/DRB3/DRB4/DRB5) | Molecular Diagnostics / PCR |
| (DSP, LMNA, SCN5A ) | (DSP, LMNA, SCN5A ) | Molecular Diagnostics / PCR |
| (ITGA2B, ITGB3) | (ITGA2B, ITGB3) | Molecular Diagnostics / PCR |
| (Illumina TruSight Cardio LMNA, SCN5A, TRPM4 ) | (Illumina TruSight Cardio LMNA, SCN5A, TRPM4 ) | 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 |
| ABO, RhD | ABO, RhD | Molecular Diagnostics / PCR |
| Afibrinogenämie (FGA, FGB, FGG) | Afibrinogenämie (FGA, FGB, FGG) | Molecular Diagnostics / PCR |
| Andersen-Tawil-Syndrom | Andersen-Tawil-Syndrom | Molecular Diagnostics / PCR |
| Angiödem (F12 ) | Angiödem (F12 ) | Molecular Diagnostics / PCR |
| Arrhythmogene Kardiomyopathie | Arrhythmogene Kardiomyopathie | Molecular Diagnostics / PCR |
| Autoimmunthrombozytopenie | Autoimmunthrombozytopenie | Molecular Diagnostics / PCR |
| Beta-Thalassämie (HBB) | Beta-Thalassämie (HBB) | Molecular Diagnostics / PCR |
| Brugada-Syndrom (Illumina Cardio Panel, SCN5A) | Brugada-Syndrom (Illumina Cardio Panel, SCN5A) | Molecular Diagnostics / PCR |
| Brugada-Syndrom (SCN5A) | Brugada-Syndrom (SCN5A) | Molecular Diagnostics / PCR |
| Cardiac Conduction Disease | Cardiac Conduction Disease | Molecular Diagnostics / PCR |
| Cumarin-Resistenz (VKORC1 CYP2C9 ) | Cumarin-Resistenz (VKORC1 CYP2C9 ) | Molecular Diagnostics / PCR |
| Cumarin-Sensitivität (CYP2C9 VKORC1 und CYP4F2 ) | Cumarin-Sensitivität (CYP2C9 VKORC1 und CYP4F2 ) | Molecular Diagnostics / PCR |
| Dilatative Kardiomyopathie | Dilatative Kardiomyopathie | Molecular Diagnostics / PCR |
| Dilatative Kardiomyopathie, (LMNA, MYH6, MYH7, MYBPC3, TNNT2, SCN5A) | Dilatative Kardiomyopathie, (LMNA, MYH6, MYH7, MYBPC3, TNNT2, SCN5A) | Molecular Diagnostics / PCR |
| Dissektionen (LOX, PRKG1) | Dissektionen (LOX, PRKG1) | Molecular Diagnostics / PCR |
| Dysfibrinogenämie (FGA, FGB, FGG) | Dysfibrinogenämie (FGA, FGB, FGG) | Molecular Diagnostics / PCR |
| Faktor XIII B-Mangel (F13B) | Faktor XIII B-Mangel (F13B) | Molecular Diagnostics / PCR |
| Faktor-V-Mangel (F5 inklusive dbSNP r6027 ) | Faktor-V-Mangel (F5 inklusive dbSNP r6027 ) | Molecular Diagnostics / PCR |
| Faktor-XIII-Mangel (F13A1 F13B); dbSNP rs5985 | Faktor-XIII-Mangel (F13A1 F13B); dbSNP rs5985 | 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 |
| Marfan-Syndrom (Illumina Cardio Panel, FBN1, TGFBR1, TGFBR2 ) | Marfan-Syndrom (Illumina Cardio Panel, FBN1, TGFBR1, TGFBR2 ) | Molecular Diagnostics / PCR |
| Morbus Glanzmann (ITGA2B ITGB3 ) | Morbus Glanzmann (ITGA2B ITGB3 ) | Molecular Diagnostics / PCR |
| Non-compaction Kardiomyopathie | Non-compaction Kardiomyopathie | Molecular Diagnostics / PCR |
| RHAG | RHAG | 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 |
| Thrombozyten, PAC-1 Bindung | Thrombozyten, PAC-1 Bindung | Molecular Diagnostics / PCR |
| TruSight Cardio Panel, KCNH2, KCNJ2, KCNQ1 | TruSight Cardio Panel, KCNH2, KCNJ2, KCNQ1 | Molecular Diagnostics / PCR |
| Weitere Blutgruppensysteme | Weitere Blutgruppensysteme | Molecular Diagnostics / PCR |
| dbSNP rs1799889 | dbSNP rs1799889 | Molecular Diagnostics / PCR |
| erythrozytäre Blutgruppenantigene, Antikörperdifferenzierung | erythrozytäre Blutgruppenantigene, Antikörperdifferenzierung | Molecular Diagnostics / PCR |
| rs1801133, dbSNP rs1801131 | rs1801133, dbSNP rs1801131 | Molecular Diagnostics / PCR |
| rs6025)Thrombophilie (F5-Gen | rs6025)Thrombophilie (F5-Gen | Molecular Diagnostics / PCR |
| sonstige Hämoglobinopathien | sonstige Hämoglobinopathien | Molecular Diagnostics / PCR |
| ventrikuläre Tachykardie | ventrikuläre Tachykardie | Molecular Diagnostics / PCR |
| weight kininogen deficiency | weight kininogen deficiency | Molecular Diagnostics / PCR |
| (DSP, LMNA, SCN5A, FLNC | (DSP, LMNA, SCN5A, FLNC | 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 |
| CASQ2, KCNJ2, CALM2, CALM3, TECRL ) | CASQ2, KCNJ2, CALM2, CALM3, TECRL ) | Other |
| Crossmatch (serologische | Crossmatch (serologische | 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 |
| Dissektionen (Illumina TruSight | Dissektionen (Illumina TruSight | Other |
| Duffy, Kidd, MNS) und seltene | Duffy, Kidd, MNS) und seltene | Other |
| Dysplasminogenämie (PLG | Dysplasminogenämie (PLG | Other |
| GP1BB, GP9 , GP5 ) | GP1BB, GP9 , GP5 ) | Other |
| Kardiomyopathie (Illumina | Kardiomyopathie (Illumina | Other |
| Kombinierter Faktor-V und | Kombinierter Faktor-V und | Other |
| MYH7, MYBPC3, TNNT2, SCN5A, DSP, FLNC ) | MYH7, MYBPC3, TNNT2, SCN5A, DSP, FLNC ) | Other |
| Mangel (GGCX und VKORC1 | Mangel (GGCX und VKORC1 | Other |
| PAI1-Mangel (PAI1= SERPINE1 dbSNP rs1799889 | PAI1-Mangel (PAI1= SERPINE1 dbSNP rs1799889 | Other |
| Plasminogen-Mangel/ | Plasminogen-Mangel/ | 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 |
| Short-QT-Syndrom (Illumina TruSight Cardio Panel, KCNH2, KCNJ2, KCNQ1 | Short-QT-Syndrom (Illumina TruSight Cardio Panel, KCNH2, KCNJ2, KCNQ1 | Other |
| Sichelzellkrankheit (HBS | Sichelzellkrankheit (HBS | Other |
| System) inklusive Auto-Crossmatch | System) inklusive Auto-Crossmatch | Other |
| TCAP, TNNC1, TPM1, GLA, FXN LAMP2, SCL25A4, TTR) | TCAP, TNNC1, TPM1, GLA, FXN LAMP2, SCL25A4, TTR) | 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 |
| (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) |
| Faktor-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) |
| 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 |
| DIN EN 13260 (2020-12) | DIN EN 13260 | Tensile / Compression / Flexural |
| DIN EN 1555-5 (2010-12) | DIN EN 1555-5 | Tensile / Compression / Flexural |
| DIN EN ISO 2244 (2002-12) | DIN EN ISO 2244 | Vibration / Shock |
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