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K-ASSAY® Alpha-1 AT Reagent

FDA UDI

Class II (US FDA UDI)

by Kamiya Biomedical Company, Llc

Identity

Trade Name
K-ASSAY® Alpha-1 AT Reagent FDA UDI
Generic Name
Trypsin-alpha-1-antitrypsin complex (elastase) IVD, reagent FDA UDI
Device Name
For the quantitative determination of human alpha-1 anti-trypsin (Alpha-1 AT) in serum by immunoturbidimetric assay. FDA UDI
Model / Reference
KAI-001 FDA UDI
Description
For the quantitative determination of human alpha-1 anti-trypsin (Alpha-1 AT) in serum by immunoturbidimetric assay. FDA UDI

Identifiers

Catalog Number
KAI-001 FDA UDI
Primary DI / UDI-DI
00816426020009 FDA UDI
510(k) Number
K993444 FDA UDI
FDA Product Code
DEM FDA UDI
GMDN Term
Trypsin-alpha-1-antitrypsin complex (elastase) IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5130 FDA UDI
Commercial Distribution
Not 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

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

K-ASSAY® Alpha-1 AT Reagent by Kamiya Biomedical Company, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 78f3a6c6-53b4-49b1-a5cd-285a28afc24a 38 fields · synced May 30, 2026