FDA UDI In Commercial Distribution 🇺🇸 United States

ALP

DI: 05055273200300 · Model: AP2809 · RANDOX LABORATORIES LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ALP
Primary DI
05055273200300
Version / Model
AP2809
Catalog Number
AP2809
Company Name
RANDOX LABORATORIES LIMITED
Labeler DUNS
227530649
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
9052fb8a-2b79-4917-83a9-8013c08d867e

Device Description

The ALP method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of Alkaline Phosphatase (ALP) activity in serum or plasma.

Device Characteristics

Single Use
Yes
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
52931 Alkaline phosphatase (ALP) isoenzyme IVD, reagent

Identifiers

Type ID
Primary 05055273200300

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K923507 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius