Skip to content

Diska Nulife

by Diska LLC

Diska Nulife is a Class II device made by Diska LLC, listed in FDA GUDID since 25 Aug 2023 (UDI-DI 00810115891710), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810115891710 UDI-DI Date25 Aug 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Glucose monitoring system IVD, home-use
Model / reference
I
Primary DI / UDI-DI
00810115891710
FDA product code
QRL
GMDN term
Glucose monitoring system IVD, home-use
Device class
Class II
Regulation number
878.4850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Glucose monitoring system IVD, home-use

Other devices from Diska LLC

See all devices from Diska LLC →

Properties

  • Supplied sterile
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)