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Ultraspec Tenaculum

EUDAMED

Class I (EU MDR)

Ref 9200

by Robinson Healthcare Ltd

Identity

Trade Name
Ultraspec Tenaculum EUDAMED
Device Name
Forceps (Tenaculum and Vulsellum) EUDAMED
Model / Reference
9200 EUDAMED

Identifiers

Primary DI / UDI-DI
05010058092006 EUDAMED
Basic UDI-DI
5010058CInT049G00CQ8 EUDAMED
EMDN Code
U089006 VAGINAL SPECULUM, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

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

Ultraspec Tenaculum by Robinson Healthcare Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
GB-MF-000016546
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 88bb4327-d8f0-42ba-9da9-0f5686b23b65 61 fields · synced Jul 9, 2026