FDA UDI In Commercial Distribution 🇺🇸 United States

LOCALISA®

DI: 00643169006874 · Model: 9670590 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LOCALISA®
Primary DI
00643169006874
Version / Model
9670590
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-30
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
f4d0b375-3710-43fa-bdca-d94405d713fb

Device Description

ELECTRODE 9670590 5BX LOCALISA

Device Characteristics

Single Use
Yes
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
DQK COMPUTER, DIAGNOSTIC, PROGRAMMABLE

GMDN Terms

Code Name
46007 Cardiac mapping system reference patch

Identifiers

Type ID
Package 20643169006878
Primary 00643169006874

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K002869 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 70 Degrees Celsius