FDA UDI In Commercial Distribution 🇺🇸 United States

The Q-TRAK™ Subcutaneous Electrode

DI: 00802526563201 · Model: 3400 · CAMERON HEALTH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
The Q-TRAK™ Subcutaneous Electrode
Primary DI
00802526563201
Version / Model
3400
Company Name
CAMERON HEALTH, INC.
Labeler DUNS
017134557
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
4
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
32e71cc3-aaa7-4fcf-93da-936eaa02f813

Device Description

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
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
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LWS Implantable cardioverter defibrillator (non-CRT)

GMDN Terms

Code Name
35853 Endocardial defibrillation lead

Identifiers

Type ID
Primary 00802526563201

Premarket Submissions

Submission Number Supplement Number
P110042 017
P110042 039