FDA UDI In Commercial Distribution 🇺🇸 United States

Revitive Arthritis Knee Pads

DI: 05060217493571 · Model: 2939 · ACTEGY LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Revitive Arthritis Knee Pads
Primary DI
05060217493571
Version / Model
2939
Catalog Number
2939
Company Name
ACTEGY LIMITED
Labeler DUNS
735575941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-28
Public Version
3
Public Version Date
2021-05-17
Public Version Status
Update
Public Device Record Key
c451ad44-e244-4bd6-97a2-53b4a6e81520

Device Description

Revitive Arthritis Knee Pads

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXY Electrode, Cutaneous

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Package 05060217493588
Primary 05060217493571
Package 05060217493663

Customer Contacts

Phone
8772603114

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
20 – 80 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
32 – 102 Degrees Fahrenheit
Type
Handling Environment Humidity
Temperature Range
20 – 80 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
32 – 102 Percent (%) Relative Humidity