ISO 9614-1:2023
Sound Power — Intensity Method (Discrete Points)
This test uses a sound intensity probe to measure acoustic intensity at discrete points on a measurement surface, allowing determination of sound power levels without requiring a fully anechoic environment. The intensity-based approach is effective for characterizing noise sources in semi-reverberant or field conditions where traditional pressure-based methods are unreliable. It provides directional acoustic information and is valuable for source localization and acoustic modification assessment. Accreditation ensures proper probe calibration, measurement procedures, and data processing are maintained to standards.
What it measures
- Sound intensity magnitude and direction (vector)
- Sound power level by surface integration
- A-weighted and frequency-weighted acoustic power
- Sound radiation patterns from complex sources
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DIN EN ISO 9614-2
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BS EN ISO 9614-2
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NF EN ISO 9614-2
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UNI EN ISO 9614-2
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UNE EN ISO 9614-2
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NEN EN ISO 9614-2
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DIN EN ISO 3744
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BS EN ISO 3744
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NF EN ISO 3744
🇮🇹
UNI EN ISO 3744
🇪🇸
UNE EN ISO 3744
🇳🇱
NEN EN ISO 3744
1,670
Accredited labs
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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
+ 3 more
Differenzierung peripheres
Erstellung eines Differentialblutbilds
Differenzierung Knochenmark
Pappenheim-Färbung
Peroxidase-Reaktion
+ 3 more
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
Hefen-Resistenz
Carbapenemasenachweis
Cryptosporidien, Giardia
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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
Arachidonsäure
Kollagen/Epinephrin
Ristocetin
Erythrozyten
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9-OH-Risperidon/Paliperidon
Aripiprazol
Citalopram
Clozapin, Norclozapin
Cyclosporin (CSA)
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Borrelia burgdorferi
Chlamydophila pneumoniae
Coxiella burnetii
Toxoplasma gondii
Adenovirus
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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
Rh-Formel
Kell-Ag
A-Untergruppe
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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
+ 3 more
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
+ 3 more
TSH
17-Hydroxyprogesteron
IRT
PAP
GALT
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Zellzahlbestimmung, CD3+, CD4+, CD8+, CD
fixpunktzellen
Phänotypisierung von Leukozyten
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
+ 3 more
Cryptococcus neoformans, Antikörper
Pneumokokken
Salmonellen
Shigella spp.
Staphylococcus aureus
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