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Single Use Guidewire MD-J-GW3505C

by Zhejiang Chuangxiang Medical Technology 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 Number06970401818815 UDI-DI Date17 Feb 2023ListedStatusListed 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  • Withdrawn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
Single Use Guidewire
Generic Name
Gastro-urological guidewire, single-use
Model / Reference
MD-J-GW3505C
Primary DI / UDI-DI
06970401818815
FDA Product Code
OCY
GMDN Term
Gastro-urological guidewire, single-use
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Gastro-urological guidewire, single-use

Other devices from Zhejiang Chuangxiang Medical Technology Co., LTD.

See all devices from Zhejiang Chuangxiang Medical Technology 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