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Injection Tubing System

by Shenzhen Antmed Co., Ltd 15 variants

Part of a family of 15 devices: see the family page

Ref 931508

Injection Tubing System (931508) is a Class IIa device made by ShenZhen Antmed Co., Ltd, registered in EUDAMED on 1 Jan 2025 (Basic UDI-DI 69457644ITS0000005MH), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69457644ITS0000005MH Basic UDI-DI 06945764440577UDI-DIDate1 Jan 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
931508
Primary DI / UDI-DI
06945764440577
Basic UDI-DI
69457644ITS0000005MH
EMDN code
A03020102 High pressure extension lines
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
CN-MF-000029659
Authorised representative
MedNet EC-REP C IIb GmbH DE-AR-000011194

Similar devices in this category

Other devices filed under HIGH PRESSURE EXTENSION LINES.

Other devices from ShenZhen Antmed Co., Ltd

See all devices from ShenZhen Antmed Co., Ltd →

Properties

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