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Bodipack+

by Sterlab 3 variants

Ref 301Model PACKS BD CHIMIQUES

Bodipack+ (301) is a Class I device made by Sterlab, registered in EUDAMED on 13 May 2022 (Basic UDI-DI 376031457BDR5), withdrawn as of 23 Oct 2026.

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376031457BDR5 Basic UDI-DI 03760314570008UDI-DIDate13 May 2022RegisteredStatusWithdrawn No longer placed on the EU market

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device name
Bowie & Dick Pack test
Model / reference
PACKS BD CHIMIQUES, 301
Primary DI / UDI-DI
03760314570008
Basic UDI-DI
376031457BDR5
EMDN code
S9080 Devices for sterilisation (excluding cat. d - z) - accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000001369

Related devices

Category: Sterilizer/disinfector rack

Similar devices in this category

Other devices filed under DEVICES FOR STERILISATION (EXCLUDING CAT. D - Z) - ACCESSORIES.

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Properties

Other properties (14, all answered No)