Identity
- Trade Name
- MyOstomy FDA UDI
- Generic Name
- Cupping therapy device FDA UDI
- Device Name
- Ostomy Suction Device, 22.5mm FDA UDI
- Model / Reference
- G4772250 FDA UDI
- Description
- Ostomy Suction Device, 22.5mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860010399705 FDA UDI
- FDA Product Code
- GCY FDA UDI
- GMDN Term
- Cupping therapy device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4680 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
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cupping therapy device
MyOstomy by Myostomy Distribution LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Tiger Warmer Large — Dong Bang Medical co., Ltd. · 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
- Myostomy Distribution LLC
Sources (1)
- FDA UDI 2abff701-ca90-4617-a51e-b09506285f62 33 fields · synced Jun 8, 2026