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Vitrification Media(BS solution) VT601US

by Kitazato Corporation

Vitrification Media(BS solution) VT601US (91109) is an IVF medium kit (FDA Class II; FDA product code MQL, Media, Reproductive) made by Kitazato Corporation, listed in FDA GUDID since 1 Nov 2019 (UDI-DI 04582231463008), 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 Number04582231463008 UDI-DI Date1 Nov 2019ListedStatusListed 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  • Withdrawn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
Vitrification Media(BS solution)
Generic name
IVF medium kit
Model / Ref / Catalog
VT601US, 91109
Primary DI / UDI-DI
04582231463008
FDA product code
MQL
GMDN term
IVF medium kit
Device class
Class II
Regulation number
884.6180
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code MQL (MEDIA, REPRODUCTIVE).

Other devices from Kitazato Corporation

See all devices from Kitazato Corporation →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)