FDA UDI In Commercial Distribution 🇺🇸 United States

FORTIFY™

DI: 05414734504386 · Model: CD2231-40Q · ST. JUDE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FORTIFY™
Primary DI
05414734504386
Version / Model
CD2231-40Q
Catalog Number
CD2231-40Q
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
8
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
802f7e9e-ce5b-43d9-ae00-44844ebbf003

Device Description

Tiered-therapy cardioverter/defibrillatorVVED DDDRV

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
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
NVZ Pulse generator, permanent, implantable

GMDN Terms

Code Name
37265 Dual-chamber implantable defibrillator

Identifiers

Type ID
Primary 05414734504386

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 35 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store the device away from magnets and sources of electromagnetic interference.
Type
Storage Environment Temperature
Temperature Range
10 – 45 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
50 – 113 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius