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B-Lite LWBI; Modular System (Gen I); B-Lite ;B-Lite/SL; B-Lite LWBI

by G&G Biotechnology Ltd. 1,000+ variants

Ref 20675-080LW25

Active European Union

CE MDD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07290109038384 Basic UDI-DI 07290109038384UDI-DIDate16 Jul 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
B-Lite LWBI
Model / Reference
20675-080LW25
Primary DI / UDI-DI
07290109038384
Basic UDI-DI
B-07290109038384
EMDN Code
P0601020202 Breast implants, anatomical, made of silicone, with textured surface
Models / Variants
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000015028
Authorised representative
MedNet EC-REP III GmbH DE-AR-000011191

Other devices from G&G Biotechnology Ltd.

See all devices from G&G Biotechnology Ltd. →

Properties

  • Sterile

Other properties (12)

  • 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