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Thromboflex

by Maco Pharma 8 variants

Ref TRV806L

Thromboflex (TRV806L) is a Class IIb device made by Maco Pharma, registered in EUDAMED on 17 Jun 2026 (Basic UDI-DI B-03567050074308), withdrawn as of 25 Oct 2026.

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03567050074308 Basic UDI-DI 03567050074308UDI-DIDate17 Jun 2026RegisteredStatusWithdrawn No longer placed on the EU market

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Withdrawn

Specification

EUDAMED

Device name
Single or multiple blood bags with TXP filter
Model / reference
TRV806L
Primary DI / UDI-DI
03567050074308
Basic UDI-DI
B-03567050074308
EMDN code
B010202 Platelets concentrate transfer bags and kits
Device class
Class IIb
EU registration type
Legacy device (under a directive)

Manufacturer details

EUDAMED SRN
FR-MF-000001657

Similar devices in this category

Other devices filed under PLATELETS CONCENTRATE TRANSFER BAGS AND KITS.

Other devices from Maco Pharma

See all devices from Maco Pharma →

Properties

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