Identity
- Trade Name
- Perma Block FDA UDI
- Generic Name
- Dental articulation paste/solution FDA UDI
- Device Name
- Perma Block Kit. Kit contains . 20 Perma Block Tips (00842092139349) . 4 Perma Block Syringes (00842092139332) FDA UDI
- Model / Reference
- 5851000 FDA UDI
- Description
- Perma Block Kit. Kit contains . 20 Perma Block Tips (00842092139349) . 4 Perma Block Syringes (00842092139332) FDA UDI
Identifiers
- Catalog Number
- 5851000 FDA UDI
- Primary DI / UDI-DI
- 00842092139356 FDA UDI
- FDA Product Code
- EBH FDA UDI
- GMDN Term
- Dental articulation paste/solution FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3670 FDA UDI
- Commercial Distribution
- Not 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
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
Perma Block by PREAT Corporation — Class I — 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 | Class I | Pending data |
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Manufacturer
- Manufacturer
- PREAT Corporation
Sources (1)
- FDA UDI d38e30ab-435e-456e-a9f6-dde69b62f537 36 fields · synced May 30, 2026