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MediTipF 21G

EUDAMED

Class IIa (EU MDR)

Ref MPS21F30

by Medicel AG

Identity

Trade Name
MediTipF 21G EUDAMED
Device Name
Phaco Accessories Set EUDAMED
Model / Reference
MPS21F30 EUDAMED

Identifiers

Primary DI / UDI-DI
07630055242662 EUDAMED
Basic UDI-DI
076300552PASU033D EUDAMED
Direct Marketing DI
07630055242662 EUDAMED
EMDN Code
Q020699 PHACOEMULSIFICATION DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa 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

MediTipF 21G by Medicel AG — Class IIa — 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
Medicel AG
EUDAMED SRN
CH-MF-000016652
Authorised Representative
Rudolf Riester GmbH DE-AR-000015844

Sources (1)

  • EUDAMED cc566935-7966-40f3-9711-fcafbee5ced8 61 fields · synced Jun 18, 2026