FDA UDI In Commercial Distribution 🇺🇸 United States

VX3+

DI: 00851074007019 · Model: VX3+ Series M · DATRIX LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VX3+
Primary DI
00851074007019
Version / Model
VX3+ Series M
Company Name
DATRIX LLC
Labeler DUNS
080555401
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
3
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
19881741-63eb-4753-9013-f396184c56b1

Device Description

Holter 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
MWJ Electrocardiograph,Ambulatory(Without Analysis)

GMDN Terms

Code Name
35162 Electrocardiographic ambulatory recorder

Identifiers

Type ID
Primary 00851074007019

Customer Contacts

Phone
651-636-9770