FDA UDI In Commercial Distribution 🇺🇸 United States

Reflexion Spiral™

DI: 05414734206211 · Model: Bi-Directional Variable Radius Catheter · ST. JUDE MEDICAL CARDIOVASCULAR DIVISION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reflexion Spiral™
Primary DI
05414734206211
Version / Model
Bi-Directional Variable Radius Catheter
Catalog Number
D402865
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
2016-01-28
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
ccbe09e3-1fbd-4002-b412-ea29c2c0b485

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
No
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 05414734206211

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K072012 000

Device Sizes

Type Value Unit Text
Catheter Gauge 7 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool dark, dry, place. Do not use if package is damaged.