AVID TruCustom ORHS014-02_0009

by Avid Medical, Inc.

AVID TruCustom ORHS014-02_0009 is a Class II device made by Avid Medical, Inc., listed in FDA GUDID since 10 Sep 2016 (UDI-DI 10809160062128), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10809160062128 UDI-DI	Date10 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10809160062128

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: AVID TruCustom
Generic name: General surgical procedure kit, medicated
Model / Ref / Catalog: ORHS014-02_0009, ORHS014-02

Primary DI / UDI-DI: 10809160062128
FDA product code: LRO
GMDN term: General surgical procedure kit, medicated

Device class: Class II
Regulation number: 878.4370
GUDID distribution status: In Commercial Distribution

Sterilisation method: Ethylene Oxide

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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)