← Back to catalogue

Apteekki Putkisidos Tubförband

EUDAMED

Class I (EU MDR)

Ref 9542032

by KOB GmbH

Identity

Trade Name
Apteekki Putkisidos Tubförband EUDAMED
Device Name
911 EUDAMED
Model / Reference
9542032 EUDAMED

Identifiers

Primary DI / UDI-DI
04004221068388 EUDAMED
Basic UDI-DI
4004221911XK EUDAMED
EMDN Code
M03030103 TUBULAR NET BANDAGES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

Apteekki Putkisidos Tubförband by KOB GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
KOB GmbH
EUDAMED SRN
DE-MF-000005043

Sources (1)

  • EUDAMED 7e82792d-caa6-4817-8971-2d4a9476c6b4 61 fields · synced Jul 15, 2026