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Bioteq

by Bioteque Corporation 1,000+ variants

Part of a family of 2,500+ devices: see the family page

Ref BT-PD2-0735

Bioteq (BT-PD2-0735) is a Class IIa device made by Bioteque Corp., registered in EUDAMED on 7 Oct 2026 (Basic UDI-DI 471988271PDZG), active as of 25 Oct 2026.

Active European Union

CE MDR

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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471988271PDZG Basic UDI-DI 04719882724480UDI-DIDate7 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Drainage Catheter Set
Model / reference
BT-PD2-0735
Primary DI / UDI-DI
04719882724480
Basic UDI-DI
471988271PDZG
EMDN code
A060299 Percutaneous drainage systems - other
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
TW-MF-000015568
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Similar devices in this category

Other devices filed under PERCUTANEOUS DRAINAGE SYSTEMS - OTHER.

Other devices from Bioteque Corp.

See all devices from Bioteque Corp. →

Properties

  • Supplied sterile
Other properties (13, all answered No)