Identity
- Trade Name
- DR-HO'S FDA UDI
- Generic Name
- Foot cushion FDA UDI
- Device Name
- Diabetic Insoles This product is used with ordinary shoes to massage the feet and relieve fatigue. FDA UDI
- Model / Reference
- DH3001 FDA UDI
- Description
- Diabetic Insoles This product is used with ordinary shoes to massage the feet and relieve fatigue. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06970742221480 FDA UDI
- FDA Product Code
- KNP FDA UDI
- GMDN Term
- Foot cushion FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3475 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Foot cushion
Dr-Ho's by Guangzhou Xinbo Electronic Co., Ltd. — 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
- Guangzhou Xinbo Electronic Co., Ltd.
Sources (1)
- FDA UDI f88797f6-4d5d-4a45-9e0c-859833b3a2aa 33 fields · synced May 30, 2026