FDA UDI Not in Commercial Distribution 🇺🇸 United States

Sprint Quattro®

DI: 00643169335585 · Model: 6946M72 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sprint Quattro®
Primary DI
00643169335585
Version / Model
6946M72
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-07
Public Version
5
Public Version Date
2023-03-16
Public Version Status
Update
Public Device Record Key
3c752b71-1c5c-4184-8d85-816cff3ce7c3
Distribution End Date
2020-11-13

Device Description

LEAD 6946M72 USA EN SPRINT DF4 PASSIVE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
35853 Endocardial defibrillation lead

Identifiers

Type ID
Primary 00643169335585

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P920015 155

Device Sizes

Type Value Unit Text
Length 72.0 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
77 – 77 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
59 – 86 Degrees Fahrenheit