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Ace

FDA UDI

Class I (US FDA UDI)

by Alfa Wassermann, Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Multiple urine analyte IVD, control FDA UDI
Device Name
Urine Chemistry Controls FDA UDI
Model / Reference
C2-85 FDA UDI
Description
Urine Chemistry Controls FDA UDI

Identifiers

Catalog Number
C2-85 FDA UDI
Primary DI / UDI-DI
00857969006419 FDA UDI
510(k) Number
K082107 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple urine analyte IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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, control

Ace by Alfa Wassermann, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple urine analyte IVD, control.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dbbec72b-e360-46a1-83d6-d990942a1c58 37 fields · synced Jun 1, 2026