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Phoenix Diagnostics, Inc. 21-109

by Phoenix Diagnostics, Inc.

Phoenix Diagnostics, Inc. 21-109 is a Class I device made by Phoenix Diagnostics, Inc., listed in FDA GUDID since 29 Jan 2018 (UDI-DI 00853366007097), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00853366007097 UDI-DI Date29 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  • Withdrawn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
Phoenix Diagnostics, Inc.
Generic name
Wash/cleaning solution IVD, automated/semi-automated system
Model / reference
21-109
Primary DI / UDI-DI
00853366007097
FDA product code
JCB
GMDN term
Wash/cleaning solution IVD, automated/semi-automated system
Device class
Class I
Regulation number
864.4010
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wash/cleaning solution IVD, automated/semi-automated system

Similar devices in this category

Other devices filed under Wash/cleaning solution IVD, automated/semi-automated system.

Other devices from Phoenix Diagnostics, Inc.

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Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)