FDA UDI In Commercial Distribution 🇺🇸 United States

Model 7A

DI: 00856233005127 · Model: Left arm patient lead wire · CARDIOCOMMAND, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Model 7A
Primary DI
00856233005127
Version / Model
Left arm patient lead wire
Catalog Number
8021
Company Name
CARDIOCOMMAND, INC.
Labeler DUNS
800214827
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-04-03
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
bece191c-652d-4c45-93d8-c77b587645ab

Device Description

Patient lead wire for use with the Model 7A stimulator; black, left arm.

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LPA System, Esophageal Pacing

GMDN Terms

Code Name
35562 Electrocardiographic lead set, reusable

Identifiers

Type ID
Primary 00856233005127

Premarket Submissions

Submission Number Supplement Number
P860008 018
P860008 022