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Tropocells® PRP

by Estar Technologies LTD. 15 variants

Ref 23GP

Tropocells PRP (23GP) is a medical device (EU MDD Class IIa; EMDN category autotransfusion singular bags) made by Estar Technologies Ltd., registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI B-07290015874922), 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-07290015874922 Basic UDI-DI 07290015874922UDI-DIDate2 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
23ml Vacuum tube with Gel, packed in Pouch
Model / reference
23GP
Primary DI / UDI-DI
07290015874922
Basic UDI-DI
B-07290015874922
EMDN code
B0101010201 Autotransfusion singular bags, w/o filters and kits
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
IL-MF-000028174
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Estar Technologies Ltd.

See all devices from Estar Technologies Ltd. →

Properties

  • Supplied sterile
Other properties (11, all answered No)