Identity
- Trade Name
- Smokeless Mini Moxa FDA UDI
- Generic Name
- Cupping therapy device FDA UDI
- Device Name
- 50 units in single package FDA UDI
- Model / Reference
- DB 207 FDA UDI
- Description
- 50 units in single package FDA UDI
Identifiers
- Primary DI / UDI-DI
- 18800018916534 FDA UDI
- FDA Product Code
- IMA FDA UDI
- GMDN Term
- Cupping therapy device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5730 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Cupping therapy device
Smokeless Mini Moxa by Dong Bang Medical co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Cupping therapy device.
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- GLASS CUP FLAT TOP NO.2 — TENS PLUS INDUSTRIAL COMPANY · Class I
- iCare Vacuum Cupping Set — Prime Holly Corporation · Class I
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
- Dong Bang Medical co., Ltd.
Sources (1)
- FDA UDI 52d320b1-a9dd-44dd-88ec-08c2ddea3fed 33 fields · synced May 30, 2026