FDA UDI In Commercial Distribution 🇺🇸 United States

Supreme™

DI: 05414734201520 · Model: 401862 · ST. JUDE MEDICAL CARDIOVASCULAR DIVISION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Supreme™
Primary DI
05414734201520
Version / Model
401862
Catalog Number
401862
Company Name
ST. JUDE MEDICAL CARDIOVASCULAR DIVISION
Labeler DUNS
040960379
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-01-26
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
703116c8-991b-42ab-ab5f-c4459db80f4b

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DRF CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING

GMDN Terms

Code Name
46355 Cardiac mapping catheter, percutaneous, single-use

Identifiers

Type ID
Primary 05414734201520

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K894500 000

Device Sizes

Type Value Unit Text
Catheter Gauge 5 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
STORE IN A COOL, DARK, DRY PLACE.