ISO 3747:2010
Sound Power Level — In-Situ Reference Source Method
This engineering/survey method determines sound power levels using a calibrated reference sound source to account for acoustic environmental conditions during in-situ measurements. It is particularly useful for large or immobile equipment where laboratory testing is impractical, and for on-site verification of noise compliance. The reference source approach compensates for acoustic environmental effects, improving accuracy compared to basic survey methods. Accreditation ensures proper reference source maintenance and measurement protocols are followed. This method is essential for field acceptance testing and environmental noise assessments.
What it measures
- Sound power level (Lw) referenced to 1 pW
- A-weighted and frequency-weighted sound power
- Environmental acoustic correction factors
- In-situ acoustic performance
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DIN EN ISO 3746
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BS EN ISO 3746
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NF EN ISO 3746
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UNI EN ISO 3746
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UNE EN ISO 3746
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NEN EN ISO 3746
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DIN EN ISO 9614-1
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BS EN ISO 9614-1
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NF EN ISO 9614-1
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UNI EN ISO 9614-1
🇪🇸
UNE EN ISO 9614-1
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NEN EN ISO 9614-1
1,670
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RPL27, RPL3, RPL31, RPL34, RPL35, RPL35A
Diamond-Blackfan-Anämie ; DBA
NOP10, PARN, RPA1, RTEL1, SAMD9, SAMD9L,
Dyskeratosis congenita; DC Panel
NOP10, PARN, POT1, RPA1, RTEL1, SAMD9, S
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Differenzierung peripheres
Erstellung eines Differentialblutbilds
Differenzierung Knochenmark
Pappenheim-Färbung
Peroxidase-Reaktion
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Universitätsklinikum Freiburg MVZ des Universitätsklinikums Freiburg, Bereich Transfusionsmedizin
Active
HLA-Antikörpertestung (Detektion)
HLA-Antikörpertestung
(Spezifizierung Klasse I und
(Spezifizierung
komplementbindender Antikörper
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Anaerobier-Resistenz
Bakterien-Resistenz
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Carbapenemasenachweis
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Thrombozyten
Zellzählung und -differenzierung
Calcium, ionisiert
Natriumchlorid
Glukose
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DPYD-Genotypisierung vor 5 FU
Therapie, SNV
Polyposissyndrome (APC, BMPR1A, MUTYH, N
(Custom made by TWIST), SNV
Hereditärer Darmkrebs inklusive
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Thrombozytenaggregation
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Kollagen/Epinephrin
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9-OH-Risperidon/Paliperidon
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Borrelia burgdorferi
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Syndrom, Gene: AKT1, PIK3CA,
PTEN, SEC23B
Carney-Komplex, Gene: PRKAR1A,
OMIM*600993, STK11
Cowden-Syndrom, Gene: AKT1,
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Blutgruppe AB0
Rh-Faktor
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DPYD (SNP-Analyse)
JAK2 Kodon 617 Mutationsanalyse
T-Zellklonalitätsanalyse (TCRG und
TCRB)
B-Zellklonalitätsanalyse (IGH, IGL, IGK)
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Aminosäuren
Second Tier Test IVA Screening
(C5 -Carnitin Isobaren)
17-α-OH-Progesteron (17-OH-P)
Biotinidase
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Factor)
Treponema pallidum-Antikörper
Treponema pallidum (TPHA)
Treponema pallidium (VDRL)
Escherichia coli Serotyp
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Cyclosporin A
Everolimus
FK 506 (Tacrolimus)
Sirolimus
6-Methylmercaptopurin
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Lymphozyten gesamt, absolut
Natürliche Killerzellen, T-Lymphozyten
Zelltypisierung (B-Lymphozyten
CD57-positive NK-Zellen
CD4+ Helfer-Lymphozyten
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Bakterien, Sprosspilze
MRGN
Streptococcus pneumoniae
Burkholderia cepacia Komplex
Bakterien, Pilze
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and Mitochondrial Panel) (BRCA1, BRCA2 )
ESR1
Punktmutation in Codons 380, 463, 535, 5
(Mammakarzinom)
OMIM*164790, PIK3CA
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TSH
17-Hydroxyprogesteron
IRT
PAP
GALT
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Zellzahlbestimmung, CD3+, CD4+, CD8+, CD
fixpunktzellen
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C3d
Faktor H
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Fragiles X-Syndrom, primäre
Tremor-Ataxie-Syndrom (FMR1
Parietalzellen/Magen)
Glutarazidurie Typ 1 (GCDH -Gen)
Dehydrogenase-Mangel (ACADM
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Acetominophen
Albumin
Alkohol
ALP
Alpha 2-Antiplasmin
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Salmonella spp.
Shigella spp.
Staphylococcus spp.
Yersinia spp.
Actinomyces spp.
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Angelmann-Syndrom (15q11-q13
Region)
Prader-Willi-Syndrom (15q11-q13
Ausschluss/ Nachweis mütterlicher
Zellen im pränatalen
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Cryptococcus neoformans, Antikörper
Pneumokokken
Salmonellen
Shigella spp.
Staphylococcus aureus
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