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Sterile Customized ProcedurePak

by Mölnlycke Health Care AB EUDAMED

Active European Union

Ref 97122848-04

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number733243000000000151JW Basic UDI-DIDate3 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
Sterile Customized ProcedurePak
Model / Reference
97122848-04
Primary DI / UDI-DI
07313662494937
Basic UDI-DI
733243000000000151JW
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class III
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.

Manufacturer details

EUDAMED SRN
SE-PR-000016902

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See all devices from Mölnlycke Health Care AB →

Properties

  • Sterile