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Disposable Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref HM101-1816ASModel HM/101-A-18/1600S

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-18/1600S EUDAMED
HM101-1816AS EUDAMED

Identifiers

Primary DI / UDI-DI
06951862210202 EUDAMED
Basic UDI-DI
B-06951862210202 EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED
R0702010101 BRONCHOSCOPIC SURGERY COLD BIOPTIC 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 — MDD — 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 78c28d7e-3211-47db-bddc-80cd187e7688 61 fields · synced Jun 19, 2026
  • EUDAMED 1944b7c7-55d5-4c02-bdaf-b732f4ad3e18 61 fields · synced Jun 19, 2026