FDA UDI In Commercial Distribution 🇺🇸 United States

Diska Nulife

DI: 00810115890782 · Model: DNL-TMB-2092-G · Diska LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Diska Nulife
Primary DI
00810115890782
Version / Model
DNL-TMB-2092-G
Company Name
Diska LLC
Labeler DUNS
006311259
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-19
Public Version
1
Public Version Date
2023-06-27
Public Version Status
New
Public Device Record Key
cd9e2f31-04fd-4ab8-9fc8-e7904aeb4061

Device Description

BP Monitor

Device Characteristics

Single Use
No
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
DXN System, Measurement, Blood-Pressure, Non-Invasive

GMDN Terms

Code Name
45617 Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

Identifiers

Type ID
Primary 00810115890782

Customer Contacts

Phone
201-675-6037