Diska Nulife TCS01

Diska Nulife TCS01 is a Class I device made by Diska LLC, listed in FDA GUDID since 25 Aug 2023 (UDI-DI 00810115891666), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00810115891666 UDI-DI	Date25 Aug 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00810115891666

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Diska Nulife
Generic name: Glucose monitoring system IVD, home-use
Model / reference: TCS01

Primary DI / UDI-DI: 00810115891666
FDA product code: JJX
GMDN term: Glucose monitoring system IVD, home-use

Device class: Class I
Regulation number: 862.1660
GUDID distribution status: In Commercial Distribution

Other devices from Diska LLC

See all devices from Diska LLC →

Properties

Single use
Premarket exempt
Lot / batch number
Expiration date
Manufacturing date

Other properties (10, all answered No)