FDA UDI In Commercial Distribution 🇺🇸 United States

Vercise Gevia™

DI: 08714729984443 · Model: DB-1200-S · BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vercise Gevia™
Primary DI
08714729984443
Version / Model
DB-1200-S
Company Name
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
Labeler DUNS
824951958
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-15
Public Version
2
Public Version Date
2021-11-03
Public Version Status
Update
Public Device Record Key
df7ff149-7874-4241-870e-c82432de68fe

Device Description

16 Contact Implantable Pulse Generator Kit

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NHL STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS
PJS Stimulator, electrical, implanted, for essential tremor
MHY Stimulator, electrical, implanted, for parkinsonian tremor

GMDN Terms

Code Name
37307 Deep brain electrical stimulation system

Identifiers

Type ID
Primary 08714729984443

Premarket Submissions

Submission Number Supplement Number
P150031 001
P150031 011
P150031 021
P150031 028
P150031 040