Skip to content

Diska Nulife DNL-VG-XL

by Diska LLC

Diska Nulife DNL-VG-XL is a Class I device made by Diska LLC, listed in FDA GUDID since 19 Jun 2023 (UDI-DI 00810115891383), 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 Number00810115891383 UDI-DI Date19 Jun 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  • Withdrawn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

Trade name
Diska Nulife
Generic name
Vinyl examination/treatment glove, non-powdered
Model / reference
DNL-VG-XL
Primary DI / UDI-DI
00810115891383
FDA product code
LYZ
GMDN term
Vinyl examination/treatment glove, non-powdered
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vinyl examination/treatment glove, non-powdered

Other devices from Diska LLC

See all devices from Diska LLC →

Properties

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