MotionWatch 04-121

GUDID B329MWR50

Ambulatory Physical Activity Recorder

CAMNTECH LIMITED

Kinesiology ambulatory recorder Kinesiology ambulatory recorder

• 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

Customer Support Contacts

• Phone: +1 830-755-8036
• Email: sales@camntech.com
• Phone: +1 830-755-8036
• Email: sales@camntech.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B329MWR50 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132764

FDA Product Code

• LEL: Device, Sleep Assessment

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-03-05
• Device Publish Date: 2018-11-02

On-Brand Devices [MotionWatch]

• B329MWR50: Ambulatory Physical Activity Recorder
• B329MW850: Ambulatory Physical Activity Recorder