FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00643169855649 · Model: A610 · MEDTRONIC, INC.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00643169855649
Version / Model
A610
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-21
Public Version
8
Public Version Date
2021-06-03
Public Version Status
Update
Public Device Record Key
a3fb17ac-b3d8-4939-99fb-8d8b2b953f5a

Device Description

SW APP A610 ACTIVA CLINICIAN DBS

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
No

Product Codes

Code Name
MHY STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR
PJS Stimulator, electrical, implanted, for essential tremor
MBX STIMULATOR, THALAMIC, EPILEPSY, IMPLANTED
MRU implanted subcortical electrical Stimulator (motor disorders)
NHL STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS
OLM Deep brain stimulator for obsessive compulsive disorder (OCD)

GMDN Terms

Code Name
61393 Multiple active implantable device programmer

Identifiers

Type ID
Primary 00643169855649

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
H020007 207
H020007 257
H020007 285
H050003 176
H050003 226
H050003 254
P960009 219
P960009 304
P960009 332
P960009 361
P960009 391