FDA UDI In Commercial Distribution 🇺🇸 United States

CARDIOBLATE®

DI: 00885074266022 · Model: 60831 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CARDIOBLATE®
Primary DI
00885074266022
Version / Model
60831
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-16
Public Version
7
Public Version Date
2024-02-08
Public Version Status
Update
Public Device Record Key
51a51915-0685-4ffc-a2f4-53f1271342f4

Device Description

CARDIOBLATE 60831 BP2 DEVICE EN

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
60784 Cardiac radio-frequency ablation system generator

Identifiers

Type ID
Primary 00885074266022

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
5 – 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius