FDA UDI In Commercial Distribution 🇺🇸 United States

mTrigger

DI: 00863712000306 · Model: AE2403 · MTRIGGER, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
mTrigger
Primary DI
00863712000306
Version / Model
AE2403
Company Name
MTRIGGER, LLC
Labeler DUNS
080226941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-28
Public Version
2
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
50b74505-fa41-4c17-b356-2ed759eab226

Device Description

Cutaneous sensing electrode - 4-pack

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
61020 Analytical non-scalp cutaneous electrode

Identifiers

Type ID
Primary 00863712000306

Customer Contacts

Phone
3025027262