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3-Stage Balloon Dilation Catheters

by Jiangsu Vedkang Medical Science and Technology Co., Ltd. 9 variants

Ref VDK-TBD-15/16.5/18-80-120

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number697005757012HB Basic UDI-DI 06941513203646UDI-DIDate13 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number06941513203646 UDI-DI Date20 Aug 2024ListedStatusListed GUDID: in commercial distribution

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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
3-Stage Balloon Dilation Catheters EUDAMED
VedDilator; 3-Stage Balloon Dilation Catheter GUDID
Generic Name
Gastrointestinal/biliary dilation balloon catheter, non-medicated
Model / Reference
VDK-TBD-15/16.5/18-80-120
Primary DI / UDI-DI
06941513203646
Basic UDI-DI
697005757012HB
510(k) Number
FDA Product Code
KNQ
EMDN Code
G03010199 Gastrointestinal endoscopy, balloon catheters - other
GMDN Term
Gastrointestinal/biliary dilation balloon catheter, non-medicated
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
876.5365
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
CN-MF-000008462
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Jiangsu Vedkang Medical Science and Technology Co., Ltd.

See all devices from Jiangsu Vedkang Medical Science and Technology Co., Ltd. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (18)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No