FDA UDI In Commercial Distribution 🇺🇸 United States

Intellinetix

DI: 00082161072201 · Model: 07220 · BROWNMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Intellinetix
Primary DI
00082161072201
Version / Model
07220
Company Name
BROWNMED, INC.
Labeler DUNS
091999771
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-12
Public Version
1
Public Version Date
2020-08-20
Public Version Status
New
Public Device Record Key
2b1ab7f6-775a-41f1-9395-6a922cce77f3

Device Description

Vibrating therapeutic massager

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
PM Exempt
Yes
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
ISA Massager, Therapeutic, Electric

GMDN Terms

Code Name
61096 Circulatory/musculoskeletal vibration therapy unit, hand-held

Identifiers

Type ID
Primary 00082161072201