← Back to catalogue

Single Use Hybrid Snare

EUDAMED

Class IIb (EU MDR)

Ref CH01-52023230

by Micro-Tech (Nanjing) Co., Ltd.

Identity

Device Name
Single Use Hybrid Snare EUDAMED
Model / Reference
CH01-52023230 EUDAMED

Identifiers

Primary DI / UDI-DI
06902284583078 EUDAMED
Basic UDI-DI
6902284PS58039NQ EUDAMED
EMDN Code
G03030102 POLYPECTOMY SNARES, NON-REVOLVING 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Single Use Hybrid Snare by Micro-Tech (Nanjing) Co., Ltd. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000006950
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 67fd0f96-c1b6-4d10-af3f-9f8eec7b016a 61 fields · synced Jun 19, 2026