Diska NuLife

GUDID 00810115892441

Strips

Diska LLC

Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use
Primary Device ID00810115892441
NIH Device Record Keydd228c67-5ea6-4ad7-aea8-58f5326f0d89
Commercial Distribution StatusIn Commercial Distribution
Brand NameDiska NuLife
Version Model NumberVGS01 (REF: DNL-VGS01)
Company DUNS006311259
Company NameDiska LLC
Device Count50
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810115892427 [Primary]
GS100810115892434 [Unit of Use]
GS100810115892441 [Package]
Contains: 00810115892427
Package: Case [200 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NBWSystem, Test, Blood Glucose, Over The Counter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-13
Device Publish Date2023-10-05

On-Brand Devices [Diska NuLife]

00810115891246Blue Nitrile Gloves - Single box(Large)
00810115891390Clear Vinyl Gloves - Single box(X-large)
00810115891338Clear Vinyl Gloves - Single box (Medium)
00810115891307Clear Vinyl Gloves - Single box(small)
00810115891277Blue Nitrile Gloves - Single box(X-large)
00810115891215Blue Nitrile Gloves - Single box (Medium)
00810115891185Blue Nitrile Gloves - Single box(small)
00810115891154Black Nitrile gloves - Single box(X-large)
00810115891123Black Nitrile gloves - Single box(Large)
00810115891093Black Nitrile gloves - Single box (Medium)
00810115891062Black Nitrile gloves - Single box(small)
00810115891406Weight scale
00810115890782BP Monitor
00810115891369Clear Vinyl Gloves - Single box(Large)
00810115891734Single Use Lancets
00810115891703Blood Glucose Test Strips
00810115891673Control Solution
00810115891659Lancing Device
00810115891598Blood Glucose Meter
00810115892465Control Solution
00810115892441Strips
00810115892403BLE Pulse Oximeter
00810115892373BLE Weight Scale with Glass Platform
00810115892359BLE Glucometer
00810115892335BLE Blood Pressure Monitor

Trademark Results [Diska NuLife]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DISKA NULIFE
DISKA NULIFE
97134370 not registered Live/Pending
Diska LLC
2021-11-19
DISKA NULIFE
DISKA NULIFE
88916035 not registered Live/Pending
DISKA LLC
2020-05-14

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