FDA UDI In Commercial Distribution 🇺🇸 United States

Senza®

DI: 00813426020008 · Model: NIPG1000 · NEVRO CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Senza®
Primary DI
00813426020008
Version / Model
NIPG1000
Catalog Number
NIPG1000
Company Name
NEVRO CORP.
Labeler DUNS
926599155
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-05-21
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
cff739ed-d67c-4c70-9456-987f754ece45

Device Description

Senza IPG Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
Yes
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
36007 Analgesic spinal cord electrical stimulation system

Identifiers

Type ID
Primary 00813426020008

Customer Contacts

Phone
6502510005

Premarket Submissions

Submission Number Supplement Number
P130022 000