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Sterile Customized ProcedurePak

EUDAMED

Class IIa (EU MDR)

Ref 97052352-05

by Mölnlycke Health Care AB

Identity

Device Name
Sterile Customized ProcedurePak EUDAMED
Model / Reference
97052352-05 EUDAMED

Identifiers

Primary DI / UDI-DI
07313662450629 EUDAMED
Basic UDI-DI
733243000000000133JU EUDAMED
EMDN Code
V0599 CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Medical Purpose
The intention of co-packing components into trays is to replace a large number of individually packaged items and generate savings in time for surgery procedures. EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

Sterile Customized ProcedurePak by Mölnlycke Health Care AB — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical procedure kit, non-medicated, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
SE-PR-000016902

Sources (1)

  • EUDAMED de2c5dfe-ef42-4cb8-b7c5-6f8d49f02f9a 61 fields · synced Oct 6, 2026