FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00763000059385 · Model: 6719 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00763000059385
Version / Model
6719
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-22
Public Version
3
Public Version Date
2021-03-19
Public Version Status
Update
Public Device Record Key
81276a71-1d33-4875-b5b0-54358b0dcf33

Device Description

PIN PLUG 6719 CONNCTR PORT OUS US EIFU

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LWS Implantable cardioverter defibrillator (non-CRT)
NVY Permanent defibrillator electrodes

GMDN Terms

Code Name
44900 Implantable pulse generator port plug

Identifiers

Type ID
Primary 00763000059385

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P920015 113

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius