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KIRO Link 1006

by Kiro Grifols Sl.

KIRO Link 1006 is a Class I device made by Kiro Grifols Sl., listed in FDA GUDID since 7 Nov 2018 (UDI-DI 08437014572308), 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 Number08437014572308 UDI-DI Date7 Nov 2018ListedStatusListed 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  • Withdrawn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
KIRO Link
Generic name
Medical equipment non-clinical data monitoring software
Model / reference
1006
Primary DI / UDI-DI
08437014572308
FDA product code
OUG
GMDN term
Medical equipment non-clinical data monitoring software
Device class
Class I
Regulation number
880.6310
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical equipment non-clinical data monitoring software

Similar devices

Other devices filed under FDA product code OUG (Medical Device Data System).

Other devices from Kiro Grifols Sl.

Properties

  • Premarket exempt
Other properties (14, all answered No)