FDA UDI Not in Commercial Distribution 🇺🇸 United States

CARDIOBLATE®

DI: 00885074243092 · Model: 60884 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CARDIOBLATE®
Primary DI
00885074243092
Version / Model
60884
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-02
Public Version
6
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
92bf5d59-9695-41d2-a623-4439965edf2a
Distribution End Date
2017-08-25

Device Description

ADAPTER 60884 DISP ELEC ADPTR 15 LANG

Device Characteristics

Single Use
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
OCL Surgical Device, For cutting, coagulation, and/or ablation of tissue, including cardiac tissue

GMDN Terms

Code Name
60784 Cardiac radio-frequency ablation system generator

Identifiers

Type ID
Primary 00885074243092

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K043291 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Maximum storage temperature: 49°C.