FDA UDI In Commercial Distribution 🇺🇸 United States

PulseSelect™

DI: 00763000617783 · Model: PSFS100 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PulseSelect™
Primary DI
00763000617783
Version / Model
PSFS100
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-10
Public Version
1
Public Version Date
2024-02-19
Public Version Status
New
Public Device Record Key
43177518-7624-43c5-8d5e-ca1d311f7362

Device Description

FOOTSWITCH PSFS100 PFA US

Device Characteristics

Single Use
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QZI Percutaneous Cardiac Ablation Catheter for Treatment of Atrial Fibrillation with Irreversible Electroporation

GMDN Terms

Code Name
36336 Foot-switch, electrical

Identifiers

Type ID
Primary 00763000617783

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P230017 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry