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AVID TruCustom OCON007-08_0006

by Avid Medical, Inc.

AVID TruCustom OCON007-08_0006 is a Class II device made by Avid Medical, Inc., listed in FDA GUDID since 10 Sep 2016 (UDI-DI 10809160023181), 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 Number10809160023181 UDI-DI Date10 Sep 2016ListedStatusListed 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  • Withdrawn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
Birthing/delivery kit
Model / reference
OCON007-08_0006
Primary DI / UDI-DI
10809160023181
FDA product code
OKV
GMDN term
Birthing/delivery kit
Device class
Class II
Regulation number
884.4520
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Birthing/delivery kit

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)