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Twist Lancet (31G) LF-TL-31

by Shandong Lianfa Medical Plastic Products CO., LTD 24 variants

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 Number06949517000667 UDI-DI Date30 Apr 2019ListedStatusListed 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  • Withdrawn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
Twist Lancet (31G)
Generic Name
Blood lancet, single-use
Model / Reference
LF-TL-31
Primary DI / UDI-DI
06949517000667
FDA Product Code
FMK
GMDN Term
Blood lancet, single-use
Device Class
Class II
Regulation Number
878.4850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood lancet, single-use

Other devices from Shandong Lianfa Medical Plastic Products Co., Ltd.

See all devices from Shandong Lianfa Medical Plastic Products Co., Ltd. →

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

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