Primary Device ID | 15099590542474 |
NIH Device Record Key | 740af675-12ea-4d0f-ba82-2a4409a60ff2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CS/CC CD3(IgG1)-FITC/T4-RD1 |
Version Model Number | 6604929 |
Catalog Number | 6604929 |
Company DUNS | 008254708 |
Company Name | Beckman Coulter, Inc. |
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 | true |
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 | 15099590542474 [Primary] |
GKZ | Counter, Differential Cell |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-23 |
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