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Angioway LP-P-30-YNP

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

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06936733735930 UDI-DI Date23 May 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Angioway
Generic Name
Catheter/overtube balloon inflator, single-use
Model / Reference
LP-P-30-YNP
Primary DI / UDI-DI
06936733735930
FDA Product Code
PTL, DTL, PTM
GMDN Term
Catheter/overtube balloon inflator, single-use
Device Class
Class II
Regulation Number
870.1330, 870.4290, 870.1650
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