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Quantib ND 1.7

by Quantib B.V.

Quantib ND 1.7 is a Class II device made by Quantib B.V., listed in FDA GUDID since 28 Nov 2020 (UDI-DI 08719689791094), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08719689791094 UDI-DI Date28 Nov 2020ListedStatusListed 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  • Withdrawn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
Quantib ND
Generic name
MRI system application software
Model / reference
1.7
Primary DI / UDI-DI
08719689791094
FDA product code
LLZ
GMDN term
MRI system application software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: MRI system application software

Similar devices in this category

Other devices filed under MRI system application software.

Other devices from Quantib B.V.

  • Quantib AI Node 2.4

    Class II

  • Quantib AI Node 2.2

    Class II

  • Quantib Prostate 2.0

    Class II

  • Quantib ND 2.2

    Class II

See all devices from Quantib B.V. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)