Primary Device ID | 00822383988399 |
NIH Device Record Key | cee4fab1-a4a7-47aa-a852-70e0c4f57ac9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Drive |
Version Model Number | 15005LP |
Company DUNS | 867673159 |
Company Name | Drive Devilbiss Healthcare |
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 | 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 | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00822383988399 [Primary] |
FNL | BED, AC-POWERED ADJUSTABLE HOSPITAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-12-17 |
Device Publish Date | 2018-11-16 |
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