FDA UDI In Commercial Distribution 🇺🇸 United States

ACTIVA RC

DI: 00643169529779 · Model: 37612 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACTIVA RC
Primary DI
00643169529779
Version / Model
37612
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-01
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
baec76c3-27a8-446f-9e2c-cb1772441908

Device Description

INS 37612 ACTIVA RC NO PARYLENE PAPR MAN

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
NHL STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS
MHY STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR

GMDN Terms

Code Name
37307 Deep brain electrical stimulation system

Identifiers

Type ID
Primary 00643169529779

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P960009 149

Storage Conditions

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