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MENTOR SILTEX CONTOUR PROFILE BECKER 35 Expander / Gel Breast Implant Cohesive II

by Mentor Medical Systems B.V. 4 variants

Ref 324-1055Model MENTOR BECKER Expanders/ Breast Implants

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8717694a00001S3 Basic UDI-DI 08717694014603UDI-DIDate26 Feb 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  • Withdrawn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
MENTOR BECKER Expanders/ Breast Implants
Model / Reference
MENTOR BECKER Expanders/ Breast Implants, 324-1055
Primary DI / UDI-DI
08717694014603
Basic UDI-DI
8717694a00001S3
EMDN Code
P060201 Breast implants, becker type
Device Class
Class III
Medical Purpose
The intended purpose of the Mentor Becker Expander/Breast Implants is to perform tissue expansion and replace missing breast tissue or to enhance a breast in females undergoing breast augmentation (non-medical purpose) or breast reconstruction (medical purpose).

Manufacturer details

EUDAMED SRN
NL-PR-000013793

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Properties

Other properties (1)

  • Sterile: No