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Aadco Db-5030

by Aadco Medical, Inc.

Aadco Db-5030 is a Class I device made by Aadco Medical, Inc., listed in FDA GUDID since 19 Dec 2022 (UDI-DI 00840348525892), 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 Number00840348525892 UDI-DI Date19 Dec 2022ListedStatusListed 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  • Withdrawn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
Aadco
Generic name
Sterilization packaging, single-use
Model / Ref / Catalog
DB-5030
Primary DI / UDI-DI
00840348525892
FDA product code
IWQ
GMDN term
Sterilization packaging, single-use
Device class
Class I
Regulation number
892.6500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sterilization packaging, single-use

Other devices from Aadco Medical, Inc.

See all devices from Aadco Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)