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Angioway LP-P-30S-YNP50H

by Lepu Medical Technology (Beijing) Co., Ltd.

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

CE MDR

Valid until

Not listed

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number06936733736159 UDI-DI Date23 May 2018ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number— Date—StatusActive

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  • Withdrawn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
Angioway
Generic Name
Catheter/overtube balloon inflator, single-use
Model / Reference
LP-P-30S-YNP50H
Primary DI / UDI-DI
06936733736159
FDA Product Code
PTM, DTL
GMDN Term
Catheter/overtube balloon inflator, single-use
Device Class
Class II
Regulation Number
870.1650, 870.4290
GUDID distribution status
In Commercial Distribution

Related devices

Category: Catheter/overtube balloon inflator, single-use

Other devices from Lepu Medical Technology (Beijing) Co., Ltd.

See all devices from Lepu Medical Technology (Beijing) Co., Ltd. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No