Hain Lifescience GmbH
Germany Last updated 8 Jun 2026
- Devices
- 79
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
FluoroCycler® XT Ref 2017
micro-IDent® VER 2.0 Ref 23296
Analyzer LA Gastrointestinal 2 PCR 1 Ref 1915176
FluoroType® STI VER 1.0 Ref 1877362
GXT Blood Extraction Kit VER 2.0 Ref 12.07.02
ThromboType® VER 2.0 Ref 24196
Analyzer GENERIC HIV-1 VL 2.0 FCXT Ref 1913150
Proteinase K Set VER 1.0 Ref 1876673
GenoType MTBDRsl VER 2.0 Ref 317A
Inactivation Set VER 1.0 Ref 522960
FluoroType® HLA-B27 VER 1.0 Ref 60896
GenoType CVD VER 1.0 Ref 33512
GenoType HelicoDR VER 1.0 Ref 337
FluoroType® CT VER 1.0 Ref 61096
FluoroType® SARS-CoV-2/Flu/RSV VER 1.0 Ref 1880015
FluoroType® MRSA VER 3.0 Ref 62596
GT-Blot 48 Ref 1003/1
FluoroType® Mycobacteria VER 1.0 Ref 1880017
GXT96 X2 Extraction Kit VER 1.0 Ref 520960
X2 Cartridge VER 1.0 Ref 12.02.02
Geno•card Ver 1.0 Ref G00196
GenoType MTBDRsl VER 2.0 Ref 31796A
LiquidArray® MTB-XDR VER 1.0 Ref 1880018
GenoXtract® fleXT Software Ref 1896938
GenoType MTBC VER 1.X Ref 301
GenoXtract® Ref 8.31.01
GXT96 X3 Extraction Kit VER 1.0 Ref 550960
Stool Buffer VER 1.0 Ref 1897036
GenoType LCT VER 1.0 Ref 261
TwinCubator Ref 7025009
SW Set VER 1.0 Ref H-270
LiquidArray® Gastrointestinal VER 1.0 Ref 1896297
Analyzer LA Gastrointestinal PCR 2 Ref 1909945
ThromboType®plus VER 3.0 Ref 341
GenoType CMdirect VER 1.0 Ref 295
Analyzer FT MTBDR 2.0 FC XT Ref 1915203
GenoType NTM-DR VER 1.0 Ref 29712
GTQ-Cycler 96 Ref 1876820
GenoType Mycobacterium CM VER 2.0 Ref 299A
GenoLyse VER 1.0 Ref 51610
GXT NA Extraction Kit VER 1.0 Ref 12.08.02
FluoroType® HH C282Y VER 1.0 Ref 60624
WorklistGenerator Ref 1896936
GenoType LepraeDR VER 1.0 Ref 320
GenoType Mycobacterium CM VER 2.0 Ref 29996A
GenoType MTBDRplus VER 2.0 Ref 304A
FluoroSoftware® IVD Ref 1897069
ThromboType® VER 2.0 Ref 241
LiquidArray® Gastrointestinal VER 2.0 Ref 1910680
Showing 1-50 of 79
EUDAMED certificates
TÜV SÜD Product Service GmbH 0123 2 certificates
- V70 079456 0011 Issued
Technical documentation EU IVDR
- Issued
- 28 Jan 2025
- Expires
- 27 Jan 2030
- V70 079456 0010 Issued
Technical documentation EU IVDR
- Issued
- 4 Mar 2024
- Expires
- 3 Mar 2029
Related companies
Notified bodies
Frequently asked questions
How many devices does Hain Lifescience GmbH have in the registry?
The registry currently lists 79 devices for Hain Lifescience GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hain Lifescience GmbH's devices?
Among its 50 most recently registered devices, Hain Lifescience GmbH has devices listed in EUDAMED (50 devices).
What risk classes do Hain Lifescience GmbH's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Hain Lifescience GmbH's devices are IVDR Class A, IVDR Class C, IVD general and IVD Annex II List B. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Hain Lifescience GmbH?
EUDAMED lists 2 certificates for Hain Lifescience GmbH (technical documentation) under IVDR. 2 are recorded with the status issued. The most recent was issued on 2025-01-28.
What are the newest devices from Hain Lifescience GmbH in the registry?
The most recently registered devices listed for Hain Lifescience GmbH include FluoroCycler® XT, micro-IDent® VER 2.0, Analyzer LA Gastrointestinal 2 PCR 1 and FluoroType® STI VER 1.0.
Information
- Address
- 1, Hardwiesenstraße, Nehren, Germany
- Website
- bruker.com
- [email protected]
- EUDAMED SRN
- DE-MF-000008606