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CORONET® EndoGlide™

EUDAMED

Class IIa (EU MDR)

Ref 51-826Model CORONET® DMEK EndoGlide™Ref 51-823Model CORONET® EndoGlide™ Ultrathin

by Network Medical Products Limited

Identity

Trade Name
CORONET® EndoGlide™ EUDAMED
Device Name
CORONET® EndoGlide™ Corneal Tissue Delivery System EUDAMED
Model / Reference
CORONET® DMEK EndoGlide™ EUDAMED
51-826 EUDAMED
CORONET® EndoGlide™ Ultrathin EUDAMED
51-823 EUDAMED

Identifiers

Primary DI / UDI-DI
05056100704442 EUDAMED
05060165019335 EUDAMED
Basic UDI-DI
B-05056100704442 EUDAMED
B-05060165019335 EUDAMED
EMDN Code
Q020299 CORNEA EXPLANTATION AND TRANSPLANTATION DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Malta EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

CORONET® EndoGlide™ by Network Medical Products Limited — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
GB-MF-000025518
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED 1547084d-071c-4208-bae5-d5933dd718e3 61 fields · synced Jul 17, 2026
  • EUDAMED 9a39bd99-b12d-4ba8-b7d9-2f6264eb6453 61 fields · synced May 18, 2026