FDA UDI In Commercial Distribution 🇺🇸 United States

Rightest

DI: 00883489001139 · Model: GM550 · BIONIME CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Rightest
Primary DI
00883489001139
Version / Model
GM550
Company Name
BIONIME CORPORATION
Labeler DUNS
658637244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-14
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
6ed6b418-ddc7-4a80-b43c-85d7634bcf82

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NBW System, Test, Blood Glucose, Over The Counter
CGA Glucose Oxidase, Glucose

GMDN Terms

Code Name
30854 Home-use/point-of-care blood glucose monitoring system IVD

Identifiers

Type ID
Package 20883489001140
Package 00883489001146
Primary 00883489001139

Premarket Submissions

Submission Number Supplement Number
K092052 000