FDA UDI Not in Commercial Distribution 🇺🇸 United States

CAPSURE®SP NOVUS

DI: 00643169590700 · Model: 509285 · MEDTRONIC, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CAPSURE®SP NOVUS
Primary DI
00643169590700
Version / Model
509285
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-01-14
Public Version
5
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
f8ba69cd-2ce2-4d60-b72e-3a75b313aed0
Distribution End Date
2018-04-18

Device Description

LEAD 509285 CAPSURE SP US BI SIL VENT

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
DTB permanent pacemaker Electrode
NVY Permanent defibrillator electrodes
NVN Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes

GMDN Terms

Code Name
35223 Endocardial pacing lead

Identifiers

Type ID
Primary 00643169590700

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P850089 110

Device Sizes

Type Value Unit Text
Length 85.0 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 104 Degrees Fahrenheit