FDA UDI In Commercial Distribution 🇺🇸 United States

Quickflex™

DI: 05414734502610 · Model: 1258T-86 · ST. JUDE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Quickflex™
Primary DI
05414734502610
Version / Model
1258T-86
Catalog Number
1258T-86
Company Name
ST. JUDE MEDICAL, INC.
Labeler DUNS
790268031
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-10
Public Version
8
Public Version Date
2022-02-23
Public Version Status
Update
Public Device Record Key
257faf11-44e1-4165-8a06-f5370624af41

Device Description

Left Heart 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
OJX Drug eluting permanent left ventricular (lv) pacemaker electrode

GMDN Terms

Code Name
35223 Endocardial pacing lead

Identifiers

Type ID
Primary 05414734502610

Customer Contacts

Device Sizes

Type Value Unit Text
Length 86 Centimeter

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-5 – 50 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
68 – 77 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Storage excursions permitted from 59°- 86° F (15°- 30°C).
Type
Handling Environment Temperature
Temperature Range
23 – 122 Degrees Fahrenheit