FDA UDI In Commercial Distribution 🇺🇸 United States

QwikCheck Dilution Kit

DI: 07290012140143 · Model: QwikCheck Dilution Kit · M.E.S. MEDICAL ELECTRONIC SYSTEMS LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
QwikCheck Dilution Kit
Primary DI
07290012140143
Version / Model
QwikCheck Dilution Kit
Company Name
M.E.S. MEDICAL ELECTRONIC SYSTEMS LTD.
Labeler DUNS
514680529
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-08
Public Version
1
Public Version Date
2023-06-16
Public Version Status
New
Public Device Record Key
b571924f-45e1-46c7-932b-ee36ff7ccc37

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KIP Formulations, Balanced Salt Solutions

GMDN Terms

Code Name
60012 Sperm energy status and motility testing reagent IVD

Identifiers

Type ID
Primary 07290012140143