Identity
- Trade Name
- G5® FDA UDI
- Generic Name
- Hand-held electric massager FDA UDI
- Device Name
- The G5 Pro-Power massager is beneficial to anyone who competes, works out, or is involved in strenuous work. Before an activity, use it to enhance flexibility, increase range-of-motion, and reduce the risk of muscle spasms, strains or contusions. After exertion, rely on the G5 Pro-Power Massager to accelerate the healing process, to reduce pain and swelling by flushing out lactic acid buildup in the muscles, and to relieve muscle pain caused by work and stress. Excellent for the relief of, repair of, and resistance to repetitive motion disorders. (Carpal Tunnel Syndrome, tendonitis, tenosynovitis, etc.) The head of the G5 Pro-Power accepts all genuine G5 Brand massage applicators. Unit Advantages: Portable: only 12" long Lightweight: weighs only 3 lbs. Hand-held device with a soft rubber grip Variable speed control: 20 - 50 cycles per second FDA UDI
- Model / Reference
- PP 24 B FDA UDI
- Description
- The G5 Pro-Power massager is beneficial to anyone who competes, works out, or is involved in strenuous work. Before an activity, use it to enhance flexibility, increase range-of-motion, and reduce the risk of muscle spasms, strains or contusions. After exertion, rely on the G5 Pro-Power Massager to accelerate the healing process, to reduce pain and swelling by flushing out lactic acid buildup in the muscles, and to relieve muscle pain caused by work and stress. Excellent for the relief of, repair of, and resistance to repetitive motion disorders. (Carpal Tunnel Syndrome, tendonitis, tenosynovitis, etc.) The head of the G5 Pro-Power accepts all genuine G5 Brand massage applicators. Unit Advantages: Portable: only 12" long Lightweight: weighs only 3 lbs. Hand-held device with a soft rubber grip Variable speed control: 20 - 50 cycles per second FDA UDI
Identifiers
- Catalog Number
- PP 24 B FDA UDI
- Primary DI / UDI-DI
- 00746980001032 FDA UDI
- FDA Product Code
- ISA FDA UDI
- GMDN Term
- Hand-held electric massager FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5660 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Weight — 3 Pound FDA UDI
Category: Hand-held electric massager
G5® by General Physiotherapy Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- General Physiotherapy Inc
Sources (1)
- FDA UDI c51f4950-6f22-41d9-9b91-e75283eb1c57 36 fields · synced Jun 6, 2026