Primary Device ID | B329MWR50 |
NIH Device Record Key | fc69a908-87aa-451e-a3f2-1bf39c25694a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MotionWatch |
Version Model Number | MW-R |
Catalog Number | 04-121 |
Company DUNS | 399114941 |
Company Name | CAMNTECH LIMITED |
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 | true |
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 |
Phone | +1 830-755-8036 |
sales@camntech.com | |
Phone | +1 830-755-8036 |
sales@camntech.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B329MWR50 [Primary] |
LEL | Device, Sleep Assessment |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-03-05 |
Device Publish Date | 2018-11-02 |
B329MWR50 | Ambulatory Physical Activity Recorder |
B329MW850 | Ambulatory Physical Activity Recorder |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MOTIONWATCH 78103476 not registered Dead/Abandoned |
e-Watch, Inc. 2002-01-18 |
MOTIONWATCH 75424431 2443006 Dead/Cancelled |
BI-STATE INVESTMENT GROUP 1, LLC 1998-01-27 |