FDA UDI In Commercial Distribution 🇺🇸 United States

Identity®

DI: 05414734006804 · Model: 5180 · ST. JUDE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Identity®
Primary DI
05414734006804
Version / Model
5180
Catalog Number
5180
Company Name
ST. JUDE MEDICAL, INC.
Labeler DUNS
790268031
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-10-23
Public Version
6
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
21b20498-e512-4697-a291-65b9539464fc

Device Description

Pulse GeneratorSSIR

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
KRG Programmer, pacemaker

GMDN Terms

Code Name
47267 Single-chamber implantable pacemaker, rate-responsive

Identifiers

Type ID
Secondary H758518006
Primary 05414734006804

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P880086 094
P880086 304
P880086 307

Device Sizes

Type Value Unit Text
Total Volume 7.9 Milliliter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-5 – 50 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
23 – 122 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
-5 – 50 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
23 – 122 Degrees Fahrenheit