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Bender +1 more model

EUDAMED

Class I (EU MDR)

Ref 397129698630

by MEDIN, a.s.

Identity

Trade Name
Bender; fissure-type, 90° EUDAMED
Device Name
Bender EUDAMED
Model / Reference
397129698630 EUDAMED

Identifiers

Primary DI / UDI-DI
08591712279638 EUDAMED
Basic UDI-DI
85917125170721Y6 EUDAMED
Direct Marketing DI
08591712279638 EUDAMED
EMDN Code
L091002 INSTRUMENTS FOR PROCESSING MATERIALS FOR OSTEOSYNTHESIS, REUSABLE EUDAMED
Models / Variants
Bender EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia 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: Wire holding/twisting forceps

Bender +1 more model by MEDIN, a.s. — Class I — MDR — listed in EUDAMED — 2 models — regulatory data on deviCERTS

Similar devices

Also classified as Wire holding/twisting forceps.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
MEDIN, a.s.
EUDAMED SRN
CZ-MF-000012371

Sources (1)

  • EUDAMED 993c7420-2cc1-492d-a5a8-467fdf88520a 61 fields · synced Jun 18, 2026