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Pipit SC

by Sahajanand Medical Technologies Limited 102 variants

Ref FGST325020

Pipit SC (FGST325020) is a Class III device made by Sahajanand Medical Technologies Limited, registered in EUDAMED on 28 Dec 2022 (Basic UDI-DI B-08904118356573), active as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08904118356573 Basic UDI-DI 08904118356573UDI-DIDate28 Dec 2022RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
FGST325020
Primary DI / UDI-DI
08904118356573
Basic UDI-DI
B-08904118356573
EMDN code
C010401020101 Ptca balloon dilation catheters
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
IN-MF-000016582
Authorised representative
Obelis s.a. BE-AR-000000106

Related devices

Category: Coronary angioplasty balloon catheter, cutting/scoring

Similar devices in this category

Other devices filed under PTCA BALLOON DILATION CATHETERS.

Other devices from Sahajanand Medical Technologies Limited

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Properties

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