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Template for A-4857.11

EUDAMED

Class I (EU MDR)

Ref A-4857.11TP

by Medartis AG

Identity

Trade Name
Template for A-4857.11 EUDAMED
Device Name
Templates EUDAMED
Model / Reference
A-4857.11TP EUDAMED

Identifiers

Primary DI / UDI-DI
07630037899112 EUDAMED
Basic UDI-DI
76300378005PA EUDAMED
EMDN Code
L091099 OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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: Surgical implant template, reusable

Template for A-4857.11 by Medartis AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Medartis AG
EUDAMED SRN
CH-MF-000022291
Authorised Representative
Medartis GmbH DE-AR-000005810

Sources (1)

  • EUDAMED 3a7523d2-8f93-4d09-a4b7-0f99a1ed5b5b 61 fields · synced Aug 4, 2026