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Autolet Plus (Blank 1-9 depth adjuster)

EUDAMED

Class I (EU MDR)

Ref 000417

by Owen Mumford Ltd

Identity

Trade Name
Autolet Plus (Blank 1-9 depth adjuster) EUDAMED
Device Name
Autolet Plus EUDAMED
Model / Reference
000417 EUDAMED

Identifiers

Primary DI / UDI-DI
05016189041739 EUDAMED
Basic UDI-DI
5016189AUTOLETPLUS6S EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Category: Blood lancet, single-use

Autolet Plus (Blank 1-9 depth adjuster) by Owen Mumford Ltd — Class I — 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 da407e44-feb5-4e8a-8488-25e5a7c17673 61 fields · synced Jul 15, 2026