← Back to catalogue

Anscare

EUDAMED

Class I (EU MDR)

Ref OS-011-1

by Cenefom Corp.

Identity

Trade Name
Anscare EUDAMED
Device Name
Ophthalmic Sponge EUDAMED
Model / Reference
OS-011-1 EUDAMED

Identifiers

Primary DI / UDI-DI
04711552922158 EUDAMED
Basic UDI-DI
471155292OPT6 EUDAMED
Direct Marketing DI
04711552922158 EUDAMED
EMDN Code
M040399 OPHTHALMIC DRESSINGS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Anscare by Cenefom Corp. — 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
Cenefom Corp.
EUDAMED SRN
TW-MF-000012190
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 48f570d7-622a-4731-944d-ef29a0069405 61 fields · synced Jul 14, 2026