FDA UDI Not in Commercial Distribution 🇺🇸 United States

MyCareLink™

DI: 00643169725379 · Model: 24950KLQ · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MyCareLink™
Primary DI
00643169725379
Version / Model
24950KLQ
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-16
Public Version
4
Public Version Date
2019-04-02
Public Version Status
Update
Public Device Record Key
43fc4628-78d6-4982-b6e4-1eca3ad68e08
Distribution End Date
2019-03-15

Device Description

MON 24950KLQ MYCARELINK/SVC USA LINQ

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OSR Pacemaker/icd/crt non-implanted components
NVZ Pulse generator, permanent, implantable

GMDN Terms

Code Name
61438 Cardiac pulse generator reader, home-use

Identifiers

Type ID
Primary 00643169725379

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P890003 369
P890003 380

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 158 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity