FDA UDI Not in Commercial Distribution 🇺🇸 United States

PrimeADVANCED™

DI: 00613994842312 · Model: 37702 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PrimeADVANCED™
Primary DI
00613994842312
Version / Model
37702
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
4
Public Version Date
2023-01-13
Public Version Status
Update
Public Device Record Key
6af22ebb-b63b-417b-82b5-2be9b295120f
Distribution End Date
2023-01-02

Device Description

INS 37702 PRIME ADV eMAN BLUE WRENCH US

Device Characteristics

Single Use
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
64970 Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable

Identifiers

Type ID
Primary 00613994842312

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P840001 159

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-18 – 52 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
0 – 126 Degrees Fahrenheit