Primary Device ID | 15099590265052 |
NIH Device Record Key | 63435954-4fb3-4e55-9ba2-3769bede45f6 |
Commercial Distribution Discontinuation | 2016-12-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | COULTER HmX |
Version Model Number | AL |
Catalog Number | 6605525 |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
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 | 15099590265052 [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 | 2019-12-23 |
Device Publish Date | 2016-09-23 |
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