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Sterile Customized ProcedurePak

by Mölnlycke Health Care AB 752 variants

Ref 97053817-39

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number733243000000000118JY Basic UDI-DI 07313662610092UDI-DIDate4 Jun 2026RegisteredStatusActive

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.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Sterile Customized ProcedurePak
Model / Reference
97053817-39
Primary DI / UDI-DI
07313662610092
Basic UDI-DI
733243000000000118JY
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class IIb
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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Properties

  • Sterile