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Unistik Touch Translucent (30G 1.5mm)

EUDAMED

Class IIa (EU MDR)

Ref 000362Ref 000361

by Owen Mumford Ltd

Identity

Trade Name
Unistik Touch Translucent (30G 1.5mm) EUDAMED
Device Name
Unistik Touch EUDAMED
Model / Reference
000362 EUDAMED
000361 EUDAMED

Identifiers

Primary DI / UDI-DI
05016189036216 EUDAMED
05016189036117 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 (30G 1.5mm) 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 5f99b000-f26e-4fe7-bae2-387a428fe62c 61 fields · synced Jul 21, 2026
  • EUDAMED b52b6fdc-ae81-46cc-a384-6eec767ffe1f 61 fields · synced May 19, 2026