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Disposable Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref HM101-2323BSModel HM/101-B-23/2300S

by Changzhou Health Microport Medical Device Co., Ltd.

Identity

Trade Name
Disposable Biopsy Forceps EUDAMED
Device Name
Disposable Biopsy Forceps EUDAMED
Model / Reference
HM/101-B-23/2300S EUDAMED
HM101-2323BS EUDAMED

Identifiers

Primary DI / UDI-DI
06951862212398 EUDAMED
Basic UDI-DI
B-06951862212398 EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland 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

Category: Flexible endoscopic biopsy forceps, single-use

Disposable Biopsy Forceps by Changzhou Health Microport Medical Device Co., Ltd — Class IIa — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000033536
Authorised Representative
Llins Service & Consulting GmbH DE-AR-000009077

Sources (2)

  • EUDAMED cdf762e1-ee3c-4c64-ae10-ead0889f6f49 61 fields · synced Oct 7, 2026
  • EUDAMED 358ce8db-1ce0-4ec3-8f72-66c1517b91d8 61 fields · synced Jul 17, 2026