FDA UDI In Commercial Distribution 🇺🇸 United States

myPatch®

DI: 00857522005095 · Model: 3 channel · DMS-SERVICE LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
30

Basic Information

Brand Name
myPatch®
Primary DI
00857522005095
Version / Model
3 channel
Catalog Number
mpE3s
Company Name
DMS-SERVICE LLC
Labeler DUNS
824740059
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2016-09-16
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
91a6e2e9-ded2-423b-b004-82b43142cdd3

Device Description

2/3 channel myPatch® electrode

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Primary 00857522005095
Unit of Use 20857522005099

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 27 Degrees Celsius