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Hot Biopsy Forceps

EUDAMED

Class IIb (EU MDR)

Ref AMH-HF-A-2.4×2000

by Anrei Medical (HZ) Co., Ltd.

Identity

Trade Name
Hot Biopsy Forceps EUDAMED
Device Name
Hot Biopsy Forceps EUDAMED
Model / Reference
AMH-HF-A-2.4×2000 EUDAMED

Identifiers

Primary DI / UDI-DI
06948318917426 EUDAMED
Basic UDI-DI
B-06948318917426 EUDAMED
EMDN Code
G0308010102 GASTROINTESTINAL ENDOSCOPY, HOT BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Hot Biopsy Forceps by Anrei Medical (HZ) CO., LTD. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000009964
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 88b24386-4a6c-4e76-a502-1baa908d1db2 61 fields · synced Jun 18, 2026