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Ace

FDA UDI

Class I (US FDA UDI)

by Alfa Wassermann, Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Low density lipoprotein (LDL) cholesterol IVD, reagent FDA UDI
Device Name
LDL-C Reagent FDA UDI
Model / Reference
RX1026 FDA UDI
Description
LDL-C Reagent FDA UDI

Identifiers

Catalog Number
RX1026 FDA UDI
Primary DI / UDI-DI
00857969006471 FDA UDI
510(k) Number
K113262 FDA UDI
FDA Product Code
MRR FDA UDI
GMDN Term
Low density lipoprotein (LDL) cholesterol IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1475 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: Low density lipoprotein (LDL) cholesterol IVD, reagent

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

Similar devices

Also classified as Low density lipoprotein (LDL) cholesterol IVD, reagent.

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 f2fb34fa-24bb-4ff5-a929-0c0c997ab4d8 37 fields · synced May 30, 2026