FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00721902309588 · Model: 5436 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00721902309588
Version / Model
5436
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
4
Public Version Date
2019-02-18
Public Version Status
Update
Public Device Record Key
6f9302d1-4f69-460f-891b-2385c8366455
Distribution End Date
2019-01-25

Device Description

CABLE 5436 PATIENT CABLE GLOBAL MR

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
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
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
NVZ Pulse generator, permanent, implantable

GMDN Terms

Code Name
47487 Electrical-only medical device connection cable, reusable

Identifiers

Type ID
Primary 00721902309588

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P890003 098

Storage Conditions

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