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Charger™ H74939206080270

by Boston Scientific

Ref H74939206080270

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

CE MDR CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number01915060000000000000344N3 Basic UDI-DI 08714729804635UDI-DIDate14 Sep 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number01915060000000000000344N3 Basic UDI-DI 08714729804635UDI-DIDate14 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08714729804635 UDI-DI Date24 Sep 2015ListedStatusListed 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.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Charger™
Generic name
Peripheral angioplasty balloon catheter, basic
Device name
Charger PTA Balloon Dilatation Catheter
Model / Ref / Catalog
H74939206080270
Primary DI / UDI-DI
08714729804635
Basic UDI-DI
01915060000000000000344N3, B-08714729804635
FDA product code
LIT, FGE
EMDN code
C010402020101 PTA balloon dilatation catheters
GMDN term
Peripheral angioplasty balloon catheter, basic
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
870.1250, 876.5010
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Related devices

Category: Peripheral angioplasty balloon catheter, basic

Other devices from Boston Scientific

See all devices from Boston Scientific →

Properties

  • Supplied sterile
  • Single use
  • Contains animal tissues or cells YesEUDAMEDNoEUDAMED
  • Prescription use
  • Lot / batch number
  • Expiration date

Other properties (19)

  • Sterilise before use: No
  • Implantable: No
  • Reusable: No
  • Contains latex: No
  • Reprocessed single-use device: No
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
  • Incorporates a substance derived from human blood or plasma: No
  • Contains human tissues or cells: No
  • Contains endocrine-disrupting substances: No
  • Administering medicine: No
  • Measuring function: No
  • Incorporates a medicinal substance: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Manufacturing date: No