FDA UDI In Commercial Distribution 🇺🇸 United States

Capsure® EPI

DI: 00613994492302 · Model: 4968-35 · MEDTRONIC, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Capsure® EPI
Primary DI
00613994492302
Version / Model
4968-35
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
5
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
7c90b7a5-0cb7-47a7-821c-41c927300071

Device Description

LEAD 4968-35 US BIPOLAR EPICARDIAL 35CM

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

GMDN Terms

Code Name
35039 Epicardial pacing lead

Identifiers

Type ID
Primary 00613994492302

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P950024 017
P950024 092

Device Sizes

Type Value Unit Text
Length 35.0 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 104 Degrees Fahrenheit