Primary Device ID | 14582231462879 |
NIH Device Record Key | 0240470d-d023-483a-89a8-3f69e24c7570 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CryotopUS-scoop(B) |
Version Model Number | CryotopUS-scoop(B) |
Catalog Number | 81198 |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04582231462872 [Primary] |
GS1 | 14582231462879 [Package] Contains: 04582231462872 Package: [10 Units] In Commercial Distribution |
MQK | LABWARE, ASSISTED REPRODUCTION |
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 | 2019-06-01 |
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