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Dau Level 2 Dau 2 Dtpm

by UTAK Laboratories Inc.

Dau Level 2 Dau 2 Dtpm is a Class I device made by UTAK Laboratories Inc., listed in FDA GUDID since 16 Mar 2023 (UDI-DI B800DAU2DTPM0), 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 NumberB800DAU2DTPM0 UDI-DI Date16 Mar 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Dau Level 2
Generic name
Multiple drugs of abuse IVD, control
Model / Ref / Catalog
DAU 2 DTPM
Primary DI / UDI-DI
B800DAU2DTPM0
FDA product code
LAS
GMDN term
Multiple drugs of abuse IVD, control
Device class
Class I
Regulation number
862.3280
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 10 Milliliter

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Properties

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