← Back to catalogue

Optimelle Incifilm

EUDAMED

Class I (EU MDR)

Ref 'FSCI059

by Pharmaplast

Identity

Trade Name
Optimelle Incifilm EUDAMED
Device Name
Incifilm® Incision drapes EUDAMED
Model / Reference
'FSCI059 EUDAMED

Identifiers

Primary DI / UDI-DI
04603727959178 EUDAMED
Basic UDI-DI
62220238Incifilm4Y EUDAMED
EMDN Code
T02010101 INCISION DRAPES, WITHOUT ANTIBACTERIAL AGENT EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Optimelle Incifilm by Pharmaplast — 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
Pharmaplast
EUDAMED SRN
EG-MF-000004501
Authorised Representative
E C REP LIMITED IE-AR-000003995

Sources (1)

  • EUDAMED 12972beb-a1fe-44d6-a873-6d9ed9831dfe 61 fields · synced Jul 25, 2026