FDA UDI In Commercial Distribution 🇺🇸 United States

Richmar TwinStim

DI: 00092237616765 · Model: DS5002 · COMPASS HEALTH BRANDS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Richmar TwinStim
Primary DI
00092237616765
Version / Model
DS5002
Company Name
COMPASS HEALTH BRANDS CORP.
Labeler DUNS
827221698
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-12
Public Version
8
Public Version Date
2023-09-08
Public Version Status
Update
Public Device Record Key
f0c2c1d0-ca89-4e6e-83e0-eeb12102db9b

Device Description

TwinStim Plus 2nd Edition

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Package 80092237616761
Primary 00092237616765

Customer Contacts

Phone
800-376-7263