FDA UDI Not in Commercial Distribution 🇺🇸 United States

AccuRelief

DI: 90002360125501 · Model: ACRL-5500 · COMPASS HEALTH BRANDS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
AccuRelief
Primary DI
90002360125501
Version / Model
ACRL-5500
Company Name
COMPASS HEALTH BRANDS CORP.
Labeler DUNS
827221698
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-12
Public Version
12
Public Version Date
2023-08-29
Public Version Status
Update
Public Device Record Key
cbe39519-508d-45b4-bbf9-c8f7ef263aa6
Distribution End Date
2019-09-01

Device Description

ULTIMATE FOOT CIRCULATOR

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Package 30023601255007
Primary 90002360125501

Customer Contacts

Phone
800-376-7263