Identity
- Trade Name
- ACTIVA™ Bio-ACTIVE-CEMENT™ FDA UDI
- Generic Name
- Dental composite resin FDA UDI
- Device Name
- SINGLE PACK: Translucent, 5mL/7gm syringe + 20 automix tips FDA UDI
- Model / Reference
- VC1T FDA UDI
- Description
- SINGLE PACK: Translucent, 5mL/7gm syringe + 20 automix tips FDA UDI
Identifiers
- Primary DI / UDI-DI
- D701VC1T2 FDA UDI
- FDA Product Code
- EJK FDA UDI
- GMDN Term
- Dental composite resin FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3250 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental composite resin
ACTIVA™ Bio-ACTIVE-CEMENT™ by Pulpdent Corporation — 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
- Pulpdent Corporation
Sources (1)
- FDA UDI ddb1ea7b-bafe-4508-9d0c-89f21a84b4e1 33 fields · synced Jun 9, 2026