FDA UDI In Commercial Distribution 🇺🇸 United States

Air Compression Therapy Device

DI: 06959557200606 · Model: ST-502 · SHENZHEN FUTURE ELECTRONIC CO.,LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Air Compression Therapy Device
Primary DI
06959557200606
Version / Model
ST-502
Company Name
SHENZHEN FUTURE ELECTRONIC CO.,LTD
Labeler DUNS
528197534
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-06
Public Version
1
Public Version Date
2022-09-14
Public Version Status
New
Public Device Record Key
471e66ca-73e2-4771-aefe-1cdfe3221ce1

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
IRP Massager, Powered Inflatable Tube

GMDN Terms

Code Name
44768 Multi-chamber venous compression system garment, reusable

Identifiers

Type ID
Primary 06959557200606

Premarket Submissions

Submission Number Supplement Number
K213745 000