FDA UDI In Commercial Distribution 🇺🇸 United States

MotionWatch

DI: B329MW850 · Model: MW8 · CAMNTECH LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MotionWatch
Primary DI
B329MW850
Version / Model
MW8
Catalog Number
04-111
Company Name
CAMNTECH LIMITED
Labeler DUNS
399114941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2020-03-05
Public Version Status
Update
Public Device Record Key
e7cd4b78-de3b-4757-9411-381e55072bce

Device Description

Ambulatory Physical Activity Recorder

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LEL Device, Sleep Assessment

GMDN Terms

Code Name
36252 Kinesiology ambulatory recorder

Identifiers

Type ID
Primary B329MW850

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K132764 000