FDA UDI In Commercial Distribution 🇺🇸 United States

Vercise™ Cartesia™ HX

DI: 08714729966357 · Model: DB-2204-30 · BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vercise™ Cartesia™ HX
Primary DI
08714729966357
Version / Model
DB-2204-30
Catalog Number
M365DB2204300
Company Name
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
Labeler DUNS
824951958
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-15
Public Version
1
Public Version Date
2024-12-23
Public Version Status
New
Public Device Record Key
c8f0fc98-5a7d-4668-96d9-2c390f38b383

Device Description

Directional Lead Kit, 16 Contact, 30cm

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
PJS Stimulator, electrical, implanted, for essential tremor
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 08714729966357

Premarket Submissions

Submission Number Supplement Number
P150031 065

Device Sizes

Type Value Unit Text
Length 30 Centimeter