FDA UDI In Commercial Distribution 🇺🇸 United States

SunMed

DI: 10889483171127 · Model: 8-1053-63 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SunMed
Primary DI
10889483171127
Version / Model
8-1053-63
Catalog Number
8-1053-63
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-01
Public Version
1
Public Version Date
2023-08-09
Public Version Status
New
Public Device Record Key
b693355a-1892-41fe-8a58-de0962c700c9

Device Description

SunStim Pro

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
BXN STIMULATOR, NERVE, BATTERY-POWERED

GMDN Terms

Code Name
35722 Block-monitoring peripheral nerve electrical stimulation system

Identifiers

Type ID
Primary 10889483171127

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K153045 000