Primary Device ID | 00853366007264 |
NIH Device Record Key | 94fe4108-0bff-4175-a6f5-0bed6c6ec1b2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PHOENIX DIAGNOSTICS, INC. |
Version Model Number | 16-221 |
Company DUNS | 606814960 |
Company Name | PHOENIX DIAGNOSTICS, INC. |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00853366007264 [Primary] |
JCB | Detergent |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-03-30 |
Device Publish Date | 2018-01-26 |
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