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Blunt Obturator

EUDAMED

Class I (EU MDR)

Ref TR2-A8EB

by Shenzhen Edge Medical Co., Ltd.

Identity

Trade Name
Blunt Obturator EUDAMED
Device Name
Obturator EUDAMED
Model / Reference
TR2-A8EB EUDAMED

Identifiers

Primary DI / UDI-DI
06975070992736 EUDAMED
Basic UDI-DI
697507099LBO00LC EUDAMED
EMDN Code
L1399 ROBOTIC SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Robotic surgical forceps, reusable

Blunt Obturator by Shenzhen Edge Medical Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Robotic surgical forceps, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000039045
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 8dc7bdf2-e7d8-47a4-9ae6-9065d8fc5833 61 fields · synced Jun 19, 2026