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Disposable Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref HM101-3023ASModel HM/101-A-30/2300S

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-A-30/2300S EUDAMED
HM101-3023AS EUDAMED

Identifiers

Primary DI / UDI-DI
06951862210899 EUDAMED
Basic UDI-DI
B-06951862210899 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 1fa27c3f-c874-4fd0-8675-798e9a564185 61 fields · synced Oct 7, 2026
  • EUDAMED cf6174b6-924a-43e9-bd5b-d860acad294b 61 fields · synced Jul 16, 2026