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Mallet

EUDAMED

Class I (EU MDR)

Ref 16-2211-24

by ABI Enterprises

Identity

Device Name
Mallet EUDAMED
Model / Reference
16-2211-24 EUDAMED

Identifiers

Primary DI / UDI-DI
*+D106162211240.* EUDAMED
Basic UDI-DI
++D106ORTHOPEDICSRB EUDAMED
EMDN Code
L091303 BONE REDUCTION FORCEPS, REUSABLE 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

Mallet by ABI Enterprises — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
ABI Enterprises
EUDAMED SRN
PK-MF-000035328
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED e314b66f-03a9-42ba-9c21-1c24135afd77 61 fields · synced Jun 19, 2026