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Corneoscleral Punch

EUDAMED

Class I (EU MDR)

Ref J-01SModel Corneoscleral PunchRef GE-328-40Ref J-011S

by CILITA Ltd.

Identity

Device Name
Corneoscleral Punch EUDAMED
Model / Reference
Corneoscleral Punch EUDAMED
J-01S EUDAMED
GE-328-40 EUDAMED
J-011S EUDAMED

Identifiers

Primary DI / UDI-DI
04610274508445 EUDAMED
04610274531818 EUDAMED
04610274508421 EUDAMED
Basic UDI-DI
468017344CILCP9Q EUDAMED
EMDN Code
L170499 OPHTHALMOLOGY SHARP INSTRUMENTS (EXCLUDING SCISSORS), REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal 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

Corneoscleral Punch by CILITA Ltd. — 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
CILITA Ltd.
EUDAMED SRN
RU-MF-000041168
Authorised Representative
Arazy Group GmbH DE-AR-000007685

Sources (3)

  • EUDAMED 1b82fa6f-f009-4610-ae53-88e2242a5ded 61 fields · synced Aug 3, 2026
  • EUDAMED 03240eb3-762a-4cdb-8985-7c76bd468321 61 fields · synced May 18, 2026
  • EUDAMED 9325f41c-a716-459e-8014-3b223185b374 61 fields · synced May 18, 2026