Primary Device ID | 00810052861173 |
NIH Device Record Key | bcf8a128-117d-44fa-99a5-cdf1d616c6cb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 642E Centrifuge, Pathology Lab Inc |
Version Model Number | 00-018-118-000 |
Catalog Number | 00-018-118-000 |
Company DUNS | 022156957 |
Company Name | DRUCKER DIAGNOSTICS |
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 | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810052861173 [Primary] |
JQC | Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-03 |
Device Publish Date | 2021-04-23 |
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