Primary Device ID | 50822383536953 |
NIH Device Record Key | 7b886928-2bef-4d07-83af-492ea77d4f4f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Drive |
Version Model Number | RTL12505 |
Company DUNS | 867673159 |
Company Name | Drive Devilbiss Healthcare |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does n |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00822383542966 [Primary] |
GS1 | 10822383536955 [Package] Package: [12 Units] In Commercial Distribution |
GS1 | 50822383536953 [Package] Contains: 00822383542966 Package: [4 Units] In Commercial Distribution |
ILS | ADAPTOR, HYGIENE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-05-19 |
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