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Trious 211T10D0

by Shenzhen Trious 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 Number06973356553961 UDI-DI Date22 Apr 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  • Withdrawn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
Trious
Generic Name
Urinary stone retrieval basket, single-use
Model / Reference
211T10D0
Primary DI / UDI-DI
06973356553961
FDA Product Code
FFL
GMDN Term
Urinary stone retrieval basket, single-use
Device Class
Class II
Regulation Number
876.4680
GUDID distribution status
In Commercial Distribution

Other devices from Shenzhen Trious Medical Technology Co., Ltd.

See all devices from Shenzhen Trious Medical Technology Co., Ltd. →

Properties

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

Other properties (8)

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