Primary Device ID | 14582231463036 |
NIH Device Record Key | b8435f09-1d36-43b8-a397-59bd797e37e5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vitrification Media(includes BS) |
Version Model Number | VT601US |
Catalog Number | 91109 |
Company DUNS | 711091157 |
Company Name | KITAZATO CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 14582231463036 [Primary] |
MQL | MEDIA, REPRODUCTIVE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-01-08 |
Device Publish Date | 2019-07-01 |
14573316384261 - BS4 - Basic Solution | 2024-05-09 Individual vial |
14573316384278 - ES4 - Equilibration Solution | 2024-05-09 Individual vial |
14573316384285 - VS4 - Vitrification Solution | 2024-05-09 Individual vial |
14573316384230 - BS - Basic Solution | 2024-05-09 Individual vial |
14573316384254 - VS - Vitrification Solution | 2024-05-09 Individual vial |
04582231462186 - Kitazato ReproPlate-K2 | 2023-09-11 1 Packs |
04582231462193 - Kitazato ReproPlate-K6 | 2023-09-11 1 Packs |
04582231462209 - Kitazato ReproPlate-K3 | 2023-09-11 1 Packs |