FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00643169508767 · Model: 5392 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00643169508767
Version / Model
5392
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-11-13
Public Version
4
Public Version Date
2018-10-05
Public Version Status
Update
Public Device Record Key
5c8cfd1d-b547-47c7-a8e2-0232b3764c65

Device Description

EPG 5392 MKT USA UPD SCREEN

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
DTE PULSE-GENERATOR, PACEMAKER, EXTERNAL

GMDN Terms

Code Name
35224 External pacemaker, epicardial pacing

Identifiers

Type ID
Primary 00643169508767

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K132924 000
K150246 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-40 – 158 Degrees Fahrenheit