FDA UDI In Commercial Distribution 🇺🇸 United States

STIMPLUS PRO

DI: 05060079210262 · Model: AC-STIMPLUS_PRO · BODY CLOCK HEALTH CARE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
STIMPLUS PRO
Primary DI
05060079210262
Version / Model
AC-STIMPLUS_PRO
Company Name
BODY CLOCK HEALTH CARE LIMITED
Labeler DUNS
504712829
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-12
Public Version
4
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
51f0469f-ec52-4082-9964-c00fa0e356a8

Device Description

The Body Clock Stimplus Pro is used for the symptomatic relief and management of chronic intractable pain and/or as an adjunctive treatment in the management of post-surgical and post-traumatic acute pain.

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
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
35372 Analgesic transcutaneous electrical nerve stimulation system

Identifiers

Type ID
Primary 05060079210262

Premarket Submissions

Submission Number Supplement Number
K041359 000