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Unistik TinyTouch Full Term

EUDAMED

Class IIa (EU MDR)

Ref AT2005

by Owen Mumford Ltd

Identity

Trade Name
Unistik TinyTouch Full Term EUDAMED
Device Name
UniStik TinyTouch EUDAMED
Model / Reference
AT2005 EUDAMED

Identifiers

Primary DI / UDI-DI
05016189200518 EUDAMED
Basic UDI-DI
5016189UNISTIKTINYTOUCHHK 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 TinyTouch Full Term 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 (1)

  • EUDAMED 097abae0-4884-4326-a089-943794e5f32e 61 fields · synced May 23, 2026