FDA UDI Not in Commercial Distribution 🇺🇸 United States

DETECT®

DI: 00613994755629 · Model: 10650 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DETECT®
Primary DI
00613994755629
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
2015-06-23
Public Version
4
Public Version Date
2018-10-05
Public Version Status
Update
Public Device Record Key
e5c0a0ea-dd20-4dd3-8e92-1fd854e3d9e6
Distribution End Date
2016-08-09

Device Description

MAPPING TOOL 10650 LES TST DETECT 5P 26L

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
Package 20613994755623
Primary 00613994755629

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K040812 000

Storage Conditions

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