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Bayflex

by Eucare Pharmaceuticals Private Limited EUDAMED

Active European Union

Ref BASP 1004, BASP 1003, BASP 1010, BASP 1001, BASP 1002, BASP 1007

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08904085093570 Basic UDI-DIDate5 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

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.

Specification

EUDAMED

Model / Reference
BASP 1004, BASP 1003, BASP 1010, BASP 1001, BASP 1002, BASP 1007
Primary DI / UDI-DI
08904085093570, 08904085093563, 08904085093631, 08904085093549, 08904085093556, 08904085093600
Basic UDI-DI
B-08904085093570, B-08904085093563, B-08904085093631, B-08904085093549, B-08904085093556, B-08904085093600
EMDN Code
M040503 Gelatine sponge haemostatic dressings
Device Class
Class III
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
IN-MF-000017539
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Eucare Pharmaceuticals Private Limited

See all devices from Eucare Pharmaceuticals Private Limited →

Properties

  • Sterile
  • Implantable
  • Animal Tissues

Other properties (8)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No