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Single Use Urethral Dilator MD-L-UD-2060

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 Number06936534328850 UDI-DI Date10 Sep 2026ListedStatusListed 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  • Withdrawn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 Urethral Dilator
Generic Name
Endoscopic-access dilator, single-use
Model / Reference
MD-L-UD-2060
Primary DI / UDI-DI
06936534328850
FDA Product Code
KOE
GMDN Term
Endoscopic-access dilator, single-use
Device Class
Class II
Regulation Number
876.5520
GUDID distribution status
In Commercial Distribution

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

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Properties

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

Other properties (7)

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