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F. Bosch Sleeve Cover PE, White

by F. Bosch International Limited

Ref PRCL-1041

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number489714698PRCLSLEEVEEN Basic UDI-DI 04897146981753UDI-DIDate21 Dec 2025RegisteredStatusActive

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  • Withdrawn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 Active

Specification

EUDAMED

Device Name
Sleevecover
Model / Reference
PRCL-1041
Primary DI / UDI-DI
04897146981753
Basic UDI-DI
489714698PRCLSLEEVEEN
Direct Marketing DI
04897146981753
EMDN Code
T0299 Protection drapes and garments - other
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
HK-MF-000029001
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from F. Bosch International Limited

See all devices from F. Bosch International Limited →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No