FDA UDI In Commercial Distribution 🇺🇸 United States

Actiwave

DI: B329AWV04E22 · Model: 4E · CAMNTECH LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Actiwave
Primary DI
B329AWV04E22
Version / Model
4E
Catalog Number
08-557
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
4
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
9e7426fb-3266-4b37-bfac-bb86c3154442

Device Description

Ambulatory ECG/EEG recorder - four channel

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
Yes
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
MWJ Electrocardiograph,Ambulatory(Without Analysis)

GMDN Terms

Code Name
38729 Telemetric electrocardiographic ambulatory recorder

Identifiers

Type ID
Primary B329AWV04E22

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K100266 000