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Pain Management 100 21070

by UTAK Laboratories Inc.

Pain Management 100 21070 is a Class I device made by UTAK Laboratories Inc., listed in FDA GUDID since 24 Feb 2020 (UDI-DI B800210700), 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 NumberB800210700 UDI-DI Date24 Feb 2020ListedStatusListed 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  • Withdrawn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
Pain Management 100
Generic name
Opiate/opiate metabolite IVD, control
Model / Ref / Catalog
21070
Primary DI / UDI-DI
B800210700
FDA product code
LAS
GMDN term
Opiate/opiate metabolite IVD, control
Device class
Class I
Regulation number
862.3280
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 5 Milliliter

Related devices

Category: Opiate/opiate metabolite IVD, control

Similar devices

Other devices filed under FDA product code LAS (Drug Specific Control Materials).

Other devices from UTAK Laboratories Inc.

See all devices from UTAK Laboratories Inc. →

Properties

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