Primary Device ID | 00718175005705 |
NIH Device Record Key | acbae2aa-b92a-423f-8828-1fa3c3175e18 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MOBILITY ASSIST |
Version Model Number | 950-570 |
Catalog Number | 950-570 |
Company DUNS | 043833813 |
Company Name | BIODEX MEDICAL SYSTEMS, 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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00718175005705 [Primary] |
BXB | Exerciser, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-06-18 |
Device Publish Date | 2019-06-10 |
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