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Mission Urinalysis Reagent Strips

FDA UDI

Class II (US FDA UDI)

by ACON Laboratories, Inc.

Identity

Trade Name
Mission Urinalysis Reagent Strips FDA UDI
Generic Name
Multiple urine analyte IVD, kit, rapid colorimetric, clinical FDA UDI
Device Name
Mission Urinalysis Reagent Strips (BLO/LEU) FDA UDI
Model / Reference
U031-021 FDA UDI
Description
Mission Urinalysis Reagent Strips (BLO/LEU) FDA UDI

Identifiers

Primary DI / UDI-DI
00682607200146 FDA UDI
FDA Product Code
JIO FDA UDI
LJX FDA UDI
GMDN Term
Multiple urine analyte IVD, kit, rapid colorimetric, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.6550 FDA UDI
864.7675 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple urine analyte IVD, kit, rapid colorimetric, clinical

Mission Urinalysis Reagent Strips by ACON Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple urine analyte IVD, kit, rapid colorimetric, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ACON Laboratories, Inc.

Sources (1)

  • FDA UDI 31fed4db-a28d-4aff-9dca-be84265865c6 35 fields · synced Jun 9, 2026