← Back to catalogue
Lamella retention insert, for matrix CM Dalbo®-Plus
FDA UDIClass II (US FDA UDI)
by ALTATEC GmbH
Identity
- Trade Name
- Lamella retention insert, for matrix CM Dalbo®-Plus FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- J2250.0007 Lamella retention insert, for matrix CM Dalbo®-Plus, d 3.3/3.8/4.3/5.0 mm FDA UDI
- Model / Reference
- J2250.0007 FDA UDI
- Description
- J2250.0007 Lamella retention insert, for matrix CM Dalbo®-Plus, d 3.3/3.8/4.3/5.0 mm FDA UDI
Identifiers
- Catalog Number
- J2250.0007 FDA UDI
- Primary DI / UDI-DI
- E219J225000071 FDA UDI
- FDA Product Code
- NHA FDA UDI
- GMDN Term
- Dental implant suprastructure, permanent, preformed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3630 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Lamella retention insert, for matrix CM Dalbo®-Plus by ALTATEC GmbH — Class II — 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- ALTATEC GmbH
Sources (1)
- FDA UDI e06e66d3-9f5d-4158-8c6a-c08e6e8a156c 36 fields · synced Jun 8, 2026