← Back to catalogue

Diska Nulife

FDA UDI

Class I (US FDA UDI)

by Diska LLC

Identity

Trade Name
Diska Nulife FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
Control Solution FDA UDI
Model / Reference
TCS01 FDA UDI
Description
Control Solution FDA UDI

Identifiers

Primary DI / UDI-DI
00810115891666 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Glucose monitoring system IVD, home-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Glucose monitoring system IVD, home-use

Diska Nulife by Diska LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose monitoring system IVD, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Diska LLC

Sources (1)

  • FDA UDI ef807354-1392-4da1-9eb9-9778489326bd 34 fields · synced May 31, 2026