FDA UDI In Commercial Distribution 🇺🇸 United States

DR -HOS

DI: 06970742220223 · Model: PBRE-I · Guangzhou Xinbo Electronic Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DR -HOS
Primary DI
06970742220223
Version / Model
PBRE-I
Company Name
Guangzhou Xinbo Electronic Co., Ltd.
Labeler DUNS
530683813
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-01
Public Version
1
Public Version Date
2022-03-09
Public Version Status
New
Public Device Record Key
9d44f870-ca9c-4fd0-a6b9-2ef755b1d17f

Device Description

Perfect Back Relief system with Electrodes

Device Characteristics

Single Use
No
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 Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Primary 06970742220223

Premarket Submissions

Submission Number Supplement Number
K202671 000