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Unistik Touch Translucent (21G 2.0mm)

EUDAMED

Class IIa (EU MDR)

Ref 000368Ref 000367

by Owen Mumford Ltd

Identity

Trade Name
Unistik Touch Translucent (21G 2.0mm) EUDAMED
Device Name
Unistik Touch EUDAMED
Model / Reference
000368 EUDAMED
000367 EUDAMED

Identifiers

Primary DI / UDI-DI
05016189036810 EUDAMED
05016189036711 EUDAMED
Basic UDI-DI
5016189UNISTIKTOUCHKF EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa 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

Category: Blood lancet, single-use

Unistik Touch Translucent (21G 2.0mm) by Owen Mumford Ltd — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Blood lancet, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Owen Mumford Ltd
EUDAMED SRN
GB-MF-000021000
Authorised Representative
Owen Mumford GmbH DE-AR-000020700

Sources (2)

  • EUDAMED f141d4bc-e8b5-4848-9c97-68fab1feceb6 61 fields · synced Jul 27, 2026
  • EUDAMED 46210eb8-3c15-4423-9e39-8f320924ec9a 61 fields · synced May 18, 2026