Primary Device ID | 00853818007033 |
NIH Device Record Key | d93dff65-fe02-4273-b605-0442a018e497 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MyoVision Wirefree System |
Version Model Number | D3-D5FL-D7 |
Catalog Number | D3-D5FL-D7 |
Company DUNS | 362997926 |
Company Name | PRECISION BIOMETRICS INC |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00853818007033 [Primary] |
KQX | Goniometer, Ac-Powered |
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 | 2016-11-15 |
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