FDA UDI Not in Commercial Distribution 🇺🇸 United States

DETECT®

DI: 00613994377890 · Model: 10650 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DETECT®
Primary DI
00613994377890
Version / Model
10650
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-21
Public Version
6
Public Version Date
2022-10-26
Public Version Status
Update
Public Device Record Key
a4176db1-65b1-4380-874e-82116ce28c06
Distribution End Date
2017-11-30

Device Description

MAPPING TOOL 10650 LES TST DETECT 5P 18L

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
LDF ELECTRODE, PACEMAKER, TEMPORARY

GMDN Terms

Code Name
35224 External pacemaker, epicardial pacing

Identifiers

Type ID
Primary 00613994377890
Package 20613994377894

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius