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Mission U120 Urine Analyzer

FDA UDI

Class I (US FDA UDI)

by ACON Laboratories, Inc.

Identity

Trade Name
Mission U120 Urine Analyzer FDA UDI
Generic Name
Urine analyser IVD, point-of-care FDA UDI
Device Name
Mission U120 Urine Analyzer with Barcode Reader FDA UDI
Model / Reference
U111-111 FDA UDI
Description
Mission U120 Urine Analyzer with Barcode Reader FDA UDI

Identifiers

Primary DI / UDI-DI
20682607200041 FDA UDI
FDA Product Code
KQO FDA UDI
GMDN Term
Urine analyser IVD, point-of-care FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urine analyser IVD, point-of-care

Mission U120 Urine Analyzer by ACON Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urine analyser IVD, point-of-care.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI df3f7727-18c0-40f8-a1ec-3f3f6c4336fd 35 fields · synced Jun 9, 2026