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Glactime®

by Advanced Medical Solutions (France) SAS 130 variants

Ref 39S35R

Glactime® (39S35R) is a Class III device made by Advanced Medical Solutions (France) SAS, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-03661522037195), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03661522037195 Basic UDI-DI 03661522037195UDI-DIDate6 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Glactime
Model / reference
39S35R
Primary DI / UDI-DI
03661522037195
Basic UDI-DI
B-03661522037195
EMDN code
H010101020201, H010101020202
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000666

Similar devices in this category

Other devices filed under POLYGLYCOLIC WITH LACTIC ACID MULTIFILAMENT.

Other devices from Advanced Medical Solutions (France) SAS

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Properties

  • Supplied sterile
  • Implantable
  • Contains animal tissues or cells
Other properties (11, all answered No)