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Mission U120 Touch Urine Analyzer U119-116-101

by Acon Laboratories, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20682607200911 UDI-DIDate6 Feb 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Mission U120 Touch Urine Analyzer
Generic Name
Urine analyser IVD, point-of-care
Model / Reference
U119-116-101
Primary DI / UDI-DI
20682607200911
FDA Product Code
CDM, JIL, JRE, JFY, JJB, CEN, JMT, JIO, JIN, JIR, KQO, LJX
GMDN Term
Urine analyser IVD, point-of-care
Device Class
Class I
Regulation Number
862.1785, 862.1340, 862.2800, 862.1225, 862.1115, 862.1550, 862.1510, 864.6550, 862.1435, 862.1645, 862.2900, 864.7675
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription Use
  • Serial Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No