Skip to content

CuffTrek LG-1

by Shanghai Longmann Tech Co., Ltd. 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number36979264200004 UDI-DI Date23 Jan 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
CuffTrek
Generic Name
Endotracheal tube cuff inflator
Model / Reference
LG-1
Primary DI / UDI-DI
36979264200004
510(k) Number
FDA Product Code
BSK
GMDN Term
Endotracheal tube cuff inflator
Device Class
Class II
Regulation Number
868.5750
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K242642)

Other devices from Shanghai Longmann Tech Co., Ltd.

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No