FDA UDI In Commercial Distribution 🇺🇸 United States

Diska Nulife

DI: 00810115891697 · Model: DNL-TTS01 · Diska LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
Diska Nulife
Primary DI
00810115891697
Version / Model
DNL-TTS01
Company Name
Diska LLC
Labeler DUNS
006311259
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2023-08-25
Public Version
1
Public Version Date
2023-09-04
Public Version Status
New
Public Device Record Key
6835bf98-6c7e-4eba-a548-b12336a03331

Device Description

Blood Glucose Test Strips

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
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
NBW System, Test, Blood Glucose, Over The Counter

GMDN Terms

Code Name
62537 Glucose monitoring system IVD, home-use

Identifiers

Type ID
Package 00810115891703
Primary 00810115891697
Unit of Use 00810115891680

Customer Contacts

Phone
201-675-6037

Premarket Submissions

Submission Number Supplement Number
K223722 000