FDA UDI In Commercial Distribution 🇺🇸 United States

OPTISURE™

DI: 05414734507288 · Model: LDP230-60 · ST. JUDE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OPTISURE™
Primary DI
05414734507288
Version / Model
LDP230-60
Catalog Number
LDP230-60
Company Name
ST. JUDE MEDICAL, INC.
Labeler DUNS
790268031
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-03
Public Version
7
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
05479a04-377c-4ea7-900c-78fede49604c

Device Description

Defibrillation Lead

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NVY Permanent defibrillator electrodes

GMDN Terms

Code Name
35853 Endocardial defibrillation lead

Identifiers

Type ID
Primary 05414734507288

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P950022 085
P950022 107

Device Sizes

Type Value Unit Text
Length 60 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
The lead should be stored at room temperature between 20C to 25C (68F to 77F). Excursions are permitted between 15C to 30C (59F to 86F).