FDA UDI In Commercial Distribution 🇺🇸 United States

Optilite Cystatin C Kit

DI: 05051700017909 · Model: LK048.OPT.A · THE BINDING SITE GROUP LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Optilite Cystatin C Kit
Primary DI
05051700017909
Version / Model
LK048.OPT.A
Company Name
THE BINDING SITE GROUP LIMITED
Labeler DUNS
347045614
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
1dc12d0e-b911-4bda-a701-0a1e0747583c

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
NDY Test, Cystatin C

GMDN Terms

Code Name
48178 Cystatin C IVD, kit, nephelometry/turbidimetry

Identifiers

Type ID
Primary 05051700017909

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K072166 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius