FDA UDI Not in Commercial Distribution 🇺🇸 United States

K-ASSAY® Fructosamine Reagent + Calibrator

DI: 00816426020238 · Model: KAI-043 · KAMIYA BIOMEDICAL COMPANY, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K-ASSAY® Fructosamine Reagent + Calibrator
Primary DI
00816426020238
Version / Model
KAI-043
Catalog Number
KAI-043
Company Name
KAMIYA BIOMEDICAL COMPANY, LLC
Labeler DUNS
197934250
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
3
Public Version Date
2019-01-01
Public Version Status
Update
Public Device Record Key
fb4a5c07-f658-4058-960c-872ad5363bf1
Distribution End Date
2018-08-28

Device Description

For the quantitative determination of fructosamine in serum.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LCP Assay, Glycosylated Hemoglobin

GMDN Terms

Code Name
53277 Fructosamine IVD, reagent

Identifiers

Type ID
Primary 00816426020238

Customer Contacts

Phone
206-575-8068

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius