FDA UDI In Commercial Distribution 🇺🇸 United States

Phoenix Diagnostics

DI: 00853366007059 · Model: 21-105 · PHOENIX DIAGNOSTICS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Phoenix Diagnostics
Primary DI
00853366007059
Version / Model
21-105
Catalog Number
21-105
Company Name
PHOENIX DIAGNOSTICS, INC.
Labeler DUNS
606814960
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-25
Public Version
4
Public Version Date
2020-03-30
Public Version Status
Update
Public Device Record Key
0d0e1d04-6e80-4f34-81dc-1e5b44ad73b4

Device Description

ISE High Serum Standard for Olympus AU Series Chemistry Systems

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
JGS Electrode, Ion Specific, Sodium
CEM Electrode, Ion Specific, Potassium
CGZ Electrode, Ion-Specific, Chloride

GMDN Terms

Code Name
52867 Multiple electrolyte IVD, calibrator

Identifiers

Type ID
Package 10853366007056
Primary 00853366007059

Customer Contacts

Phone
5086558310

Premarket Submissions

Submission Number Supplement Number
K020148 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
15 – 30 Degrees Celsius