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Instrument Kit: Fixture Removal F

EUDAMED

Class I (EU MDR)

Ref 1638

by Integrum AB

Identity

Trade Name
Instrument Kit: Fixture Removal F EUDAMED
Device Name
OPRA Implant System Instruments - OPRA Instrument Kits EUDAMED
Model / Reference
1638 EUDAMED

Identifiers

Primary DI / UDI-DI
07340152102058 EUDAMED
Basic UDI-DI
73401521RUinstrumentkit4A EUDAMED
Direct Marketing DI
07340152102058 EUDAMED
EMDN Code
L0399 GENERAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

Instrument Kit: Fixture Removal F by Integrum AB — 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
Integrum AB
EUDAMED SRN
SE-MF-000026900

Sources (1)

  • EUDAMED 2fc0c14b-9cb1-4f85-a205-e94cc013a06a 61 fields · synced Jul 10, 2026