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IUD Removal kit

EUDAMED

Class I (EU MDR)

Ref IUDKTModel IUD Kit Pack

by SMB Corporation of India

Identity

Trade Name
IUD Removal kit EUDAMED
Device Name
IUD insertion Kit EUDAMED
Model / Reference
IUD Kit Pack EUDAMED
IUDKT EUDAMED

Identifiers

Primary DI / UDI-DI
08906028600753 EUDAMED
Basic UDI-DI
890602860IUDKKC EUDAMED
EMDN Code
V901699 SPECIALIST SURGICAL INSTRUMENTS AND KITS NOT INCLUDED IN OTHER CLASSES, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

Yes

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: General internal orthopaedic fixation system implantation kit

IUD Removal kit by SMB Corporation of India — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IN-MF-000023742
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 9369a3cb-d05d-4fad-a0f7-491c1cb142fe 61 fields · synced Jun 18, 2026