Cardioblate™

GUDID 00199150027569

CARDIOBLATE 60831 BP2 DEVICE EN

MEDTRONIC, INC.

Cardiac radio-frequency ablation system generator
Primary Device ID00199150027569
NIH Device Record Key7824e4e8-5104-46e7-95cd-1851c2b1907f
Commercial Distribution StatusIn Commercial Distribution
Brand NameCardioblate™
Version Model Number60831
Company DUNS006261481
Company NameMEDTRONIC, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Operating and Storage Conditions

Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment HumidityBetween 5 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment HumidityBetween 5 Percent (%) Relative Humidity and 85 Percent (%) Relative Humidity

Device Identifiers

Device Issuing AgencyDevice ID
GS100199150027569 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, cutting & coagulation & accessories

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-01-26
Device Publish Date2026-01-16

On-Brand Devices [Cardioblate™]

00643169997974PEN 49314 CARDIOBLATE XL PEN FT
00643169997967PEN 49313 CARDIOBLATE PEN FT
00643169998018CLAMP 49341 CARDIOBLATE LP FT
00643169997998CLAMP 49321 CARDIOBLATE BP2 FT
00643169998032CLAMP 49351 CARDIOBLATE GEMINI-S FT
00199150027569CARDIOBLATE 60831 BP2 DEVICE EN
00199150027538CLAMP 49341 CARDIOBLATE LP FT
00199150027521CLAMP 49321 CARDIOBLATE BP2 FT

Trademark Results [Cardioblate]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CARDIOBLATE
CARDIOBLATE
78264538 2875737 Live/Registered
Medtronic, Inc.
2003-06-19
CARDIOBLATE
CARDIOBLATE
76017616 2672681 Dead/Cancelled
Medtronic, Inc.
2000-03-29

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.