FDA UDI In Commercial Distribution 🇺🇸 United States

PowerWire Pulse RF Guidewire Kit

DI: 07540299000457 · Model: PTK35-250-10-6S · Baylis Medical Technologies Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PowerWire Pulse RF Guidewire Kit
Primary DI
07540299000457
Version / Model
PTK35-250-10-6S
Company Name
Baylis Medical Technologies Inc
Labeler DUNS
240389677
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-27
Public Version
1
Public Version Date
2024-10-07
Public Version Status
New
Public Device Record Key
a5e3fad6-c646-4dbd-a8fe-367c7aa0b484

Device Description

PowerWire Pulse 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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

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

Identifiers

Type ID
Primary 07540299000457

Customer Contacts

Phone
905-948-5800

Premarket Submissions

Submission Number Supplement Number
K132374 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 75g straight 250cm PowerWire Pulse RF Guidewire with OD = 0.035 in, distal taper = 6cm and 5 marker bands placed 1cm apart; 3m RFP-100A Connector Cable