Identity
- Trade Name
- Delfin FDA UDI
- Generic Name
- Dental drilling system attachment FDA UDI
- Model / Reference
- DELF2-8 FDA UDI
Identifiers
- Primary DI / UDI-DI
- D742DELF2080 FDA UDI
- FDA Product Code
- EFA FDA UDI
- GMDN Term
- Dental drilling system attachment FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4200 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental drilling system attachment
Delfin by Intra-Lock International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental drilling system attachment.
- MK-dent Germany® — MK-Dent GmbH · Class I
- MK-dent Germany® — MK-Dent GmbH · Class I
- MK-dent Germany® — MK-Dent GmbH · Class I
- MK-dent Germany® — MK-Dent GmbH · Class I
- osseolink Implant — OSSEOLINK USA LLC · Class II
- osseolink Implant — OSSEOLINK USA LLC · Class II
- osseolink Implant — OSSEOLINK USA LLC · Class II
- MK-dent Germany® — MK-Dent GmbH · Class I
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
- Intra-Lock International
Sources (1)
- FDA UDI a7fca7b1-f9f2-4dad-8614-883b239df3df 32 fields · synced May 30, 2026