Identity
- Trade Name
- CXPlus FDA UDI
- Generic Name
- Glass ionomer dental cement FDA UDI
- Device Name
- CX-Plus Sample Kit. Contains DI's: E23532770 FDA UDI
- Model / Reference
- 001 FDA UDI
- Description
- CX-Plus Sample Kit. Contains DI's: E23532770 FDA UDI
Identifiers
- Catalog Number
- CX-Plus FDA UDI
- Primary DI / UDI-DI
- E235CXPLUS0 FDA UDI
- GMDN Term
- Glass ionomer dental cement FDA UDI
Classification
- Commercial Distribution
- Not 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
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
CXPlus by Shofu Dental Corp. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Shofu Dental Corp.
Sources (1)
- FDA UDI 2da6b070-a8d5-4a0b-99e3-523f3b088a32 37 fields · synced May 31, 2026