FDA UDI In Commercial Distribution 🇺🇸 United States

Diamedix

DI: 00817273020198 · Model: 720-360 · DIAMEDIX CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Diamedix
Primary DI
00817273020198
Version / Model
720-360
Company Name
DIAMEDIX CORPORATION
Labeler DUNS
151765328
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
c235302a-88aa-446b-8bab-4ecfe282e8a0

Device Description

"720-360 Rubella IgG Test Kit"

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LFX Enzyme Linked Immunoabsorbent Assay, Rubella

GMDN Terms

Code Name
50272 Rubella virus immunoglobulin G (IgG)/IgM antibody IVD, kit, fluorescent immunoassay

Identifiers

Type ID
Primary 00817273020198

Customer Contacts

Phone
305-324-2300

Premarket Submissions

Submission Number Supplement Number
K981729 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius