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Intravenous Infusion Set (Vented) with Luer Lock + Y Connector

by SBRG MedTech Pvt. Ltd.

Ref 01020401Model Infusion Set for Single Use

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number89061712501025E Basic UDI-DI 08906171250577UDI-DIDate23 Sep 2026RegisteredStatusActive

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.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Infusion Set for Single Use
Model / Reference
Infusion Set for Single Use, 01020401
Primary DI / UDI-DI
08906171250577
Basic UDI-DI
89061712501025E
EMDN Code
A03010101 Infusion controllers with or w/o air inlet
Device Class
Class IIa
EU market of registration
Estonia

Manufacturer details

EUDAMED SRN
IN-MF-000038015
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from SBRG MedTech Pvt. Ltd.

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Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No