FDA UDI In Commercial Distribution 🇺🇸 United States

PowerWire Pro Radiofrequency Guidewire Kit

DI: 07540299000396 · Model: PSK35-250-12-6A-30 · Baylis Medical Technologies Inc
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PowerWire Pro Radiofrequency Guidewire Kit
Primary DI
07540299000396
Version / Model
PSK35-250-12-6A-30
Company Name
Baylis Medical Technologies Inc
Labeler DUNS
240389677
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-18
Public Version
1
Public Version Date
2024-03-26
Public Version Status
New
Public Device Record Key
b6e20e0f-bd54-467b-a9f6-3eea21fe44d0

Device Description

PowerWire Pro RF Guidewire; RFP-100A Connector Cable

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PDU Catheter For Crossing Total Occlusions
DSA Cable, Transducer And Electrode, Patient, (Including Connector)

GMDN Terms

Code Name
61875 Endoscopic electrosurgical electrode, monopolar, single-use

Identifiers

Type ID
Primary 07540299000396

Customer Contacts

Phone
905-948-5800

Premarket Submissions

Submission Number Supplement Number
K232562 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 110 angled 30K 250cm PowerWire Pro RF Guidewire with OD = 0.035 in, distal taper = 6cm and 5 marker bands placed 1cm apart; 3m RFP-100A Connector Cable