HomeGermanyBiocheck GmbH

Biocheck GmbH

Germany · Münster · www.polycheck.de
✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
0UDI-DI device records
USUnited StatesFDA openFDA
1listed device types
Class I 0Class II 1Class III 0
plus 1 registration records and 14 510(k)
UKUnited KingdomMHRA PARD
0registered device records
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States1 registration records, 14 510(k), 0 PMA
Manufacturer names merged into this page: BIOCHECK, INC.

Company information

Country
Germany
Website
www.polycheck.de
Product categories
Clinical Diagnostics & Therapeutic TechnologiesLaboratory, IVD & DiagnosticsClinical chemistry & immunoassays

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

71999 · K992517
22000 · K002294
12001 · K003851
22002 · K022660
22004 · K041619

FDA listed device types

Brain Trauma Assessment Test 1

Registration details (sample)

MarketIdentifierNameClass / date
USK041619BIO CHECK WHOLE BLOOD/PLASMA/SERMON MODEL #8011162004-12-17
USK040030BIOCHECK CARDIAC-1 CRP RAPID TEST, MODEL BC-8041142004-06-16
USK022660BIOCHECK MYOGLOBIN ELISA, MODEL BC-11172002-12-19

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