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PERSONAL CARE Test midstream I

by Delta Brands Inc.

PERSONAL CARE Test midstream I is a Class I device made by Delta Brands Inc., listed in FDA GUDID since 16 Oct 2026 (UDI-DI 00808829132373), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00808829132373 UDI-DI Date16 Oct 2026ListedStatusListed 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  • Withdrawn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
Personal Care
Generic name
Luteinizing hormone (LH) IVD, reagent
Model / reference
Test midstream I
Primary DI / UDI-DI
00808829132373
FDA product code
NGE
GMDN term
Luteinizing hormone (LH) IVD, reagent
Device class
Class I
Regulation number
862.1485
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NGE (Test, Luteinizing Hormone (Lh), Over The Counter).

Other devices from Delta Brands Inc.

See all devices from Delta Brands Inc. →

Properties

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