FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00885074050645 · Model: 37742 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00885074050645
Version / Model
37742
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
1cecad00-c371-40bf-9ec8-5bbee4ce0130
Distribution End Date
2015-01-21

Device Description

PROGRAMMER 37742 PATIENT RX1 EN

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
LGW STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

GMDN Terms

Code Name
45252 Active-implantable-device communicator

Identifiers

Type ID
Primary 00885074050645

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P840001 074

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 65 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
-40 – 150 Degrees Fahrenheit