Identity
- Trade Name
- CERAGEM Master V9 FDA UDI
- Generic Name
- Massage table/couch, line-powered FDA UDI
- Model / Reference
- CGM MB-2401 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809643652087 FDA UDI
- FDA Product Code
- JFB FDA UDIIRP FDA UDIIRO FDA UDIISA FDA UDI
- GMDN Term
- Massage table/couch, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5880 FDA UDI890.5650 FDA UDI890.5975 FDA UDI890.5660 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
Yes
FDA UDI
Convenience Kit
No
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
Category: Compression/pressure sock/stocking, reusableSequential venous compression system inflatorMassage table/couch, line-powered
CERAGEM Master V9 by Ceragem Co., Ltd. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Ceragem Co., Ltd.
Sources (1)
- FDA UDI 2f0cfaf6-3465-4a38-8dc8-6c8086ecf9f6 32 fields · synced May 30, 2026