FDA UDI In Commercial Distribution 🇺🇸 United States

Reflexion Spiral™

DI: 05414734216654 · Model: D402893 · ST. JUDE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reflexion Spiral™
Primary DI
05414734216654
Version / Model
D402893
Catalog Number
D402893
Company Name
ST. JUDE MEDICAL, INC.
Labeler DUNS
149818952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-24
Public Version
4
Public Version Date
2023-07-31
Public Version Status
Update
Public Device Record Key
722aa157-a04b-45b6-87a8-e4f732fbb71e

Device Description

Bi-Directional Variable Radius Catheter

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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 05414734216654

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.