Primary Device ID | 10190302010337 |
NIH Device Record Key | 7552df5c-d39a-40a1-b329-685c2de68bf9 |
Commercial Distribution Discontinuation | 2023-11-29 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Human CD138 PE-Cy®5.5 Conjugate |
Version Model Number | MHCD13818 |
Company DUNS | 080131636 |
Company Name | LIFE TECHNOLOGIES CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 | 10190302010337 [Primary] |
MVU | Reagents, specific, analyte |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2023-11-30 |
Device Publish Date | 2018-05-04 |
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10190302010337 - Human CD138 PE-Cy®5.5 Conjugate | 2023-11-30 |
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