Primary Device ID | 10822383259755 |
NIH Device Record Key | 90e7fe73-d30c-42b8-9f18-a25de784eb78 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Drive |
Version Model Number | 18720 |
Company DUNS | 867673159 |
Company Name | Drive Devilbiss Healthcare |
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 | false |
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 | 00822383259758 [Primary] |
GS1 | 10822383259755 [Package] Contains: 00822383259758 Package: [50 Units] In Commercial Distribution |
DQA | Oximeter |
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 | 2016-09-16 |
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