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AVID TruCustom LIFP031_0004

by Avid Medical, Inc.

AVID TruCustom LIFP031_0004 is a Class I device made by Avid Medical, Inc., listed in FDA GUDID since 12 Jan 2018 (UDI-DI 10809160176238), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10809160176238 UDI-DI Date12 Jan 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
AVID TruCustom
Generic name
Laboratory specimen/material barcode label
Model / reference
LIFP031_0004
Primary DI / UDI-DI
10809160176238
FDA product code
LYV
GMDN term
Laboratory specimen/material barcode label
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Laboratory specimen/material barcode label

Other devices from Avid Medical, Inc.

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Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (7, all answered No)