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Sterile Customized ProcedurePak

EUDAMED

Class IIb (EU MDR)

Ref 97093830-10

by Mölnlycke Health Care AB

Identity

Device Name
Sterile Customized ProcedurePak EUDAMED
Model / Reference
97093830-10 EUDAMED

Identifiers

Primary DI / UDI-DI
07313662439624 EUDAMED
Basic UDI-DI
733243000000000114JQ EUDAMED
EMDN Code
V0599 CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class IIb 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 IIb — 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 10a8e605-fcef-4ed1-92fb-efb418f6a2f2 61 fields · synced Oct 6, 2026