Identity
- Trade Name
- INTERLIG FDA UDI
- Generic Name
- Dental reinforcing fibre FDA UDI
- Device Name
- Braided Glass Fiber Impregnated With Light-Cured Composite Resin - INTERLIG 3 units FDA UDI
- Model / Reference
- INTERLIG 3 units FDA UDI
- Description
- Braided Glass Fiber Impregnated With Light-Cured Composite Resin - INTERLIG 3 units FDA UDI
Identifiers
- Catalog Number
- 483 FDA UDI
- Primary DI / UDI-DI
- 07898078654835 FDA UDI
- 510(k) Number
- K123823 FDA UDI
- FDA Product Code
- EBF FDA UDI
- GMDN Term
- Dental reinforcing fibre FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3690 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental reinforcing fibre
Interlig by Angelus Industria de Produtos Odontologicos S A — 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
- Angelus Industria de Produtos Odontologicos S A
Sources (1)
- FDA UDI 45a1f0dd-0b43-45b6-a16e-081598eaa931 36 fields · synced May 30, 2026