FDA UDI In Commercial Distribution 🇺🇸 United States

Alkaline Phosphatase (Kinetic Procedure)

DI: 10673486001051 · Model: A505-240 · TECO DIAGNOSTICS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Alkaline Phosphatase (Kinetic Procedure)
Primary DI
10673486001051
Version / Model
A505-240
Catalog Number
A505-240
Company Name
TECO DIAGNOSTICS
Labeler DUNS
185067774
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-14
Public Version
1
Public Version Date
2023-07-24
Public Version Status
New
Public Device Record Key
46416b85-fd02-4f5e-8979-f36316bf612d

Device Description

The Alkaline Phosphatase (Kinetic Procedure) is used for the quantitative determination of alkaline phosphatase in human 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
CJE Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes

GMDN Terms

Code Name
52929 Total alkaline phosphatase (ALP) IVD, reagent

Identifiers

Type ID
Primary 10673486001051

Customer Contacts

Phone
714-463-1111

Premarket Submissions

Submission Number Supplement Number
K864905 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius