Identity
- Trade Name
- implantswiss FDA UDI
- Generic Name
- Surgical screwdriver, reusable FDA UDI
- Device Name
- Depth Gauge FDA UDI
- Model / Reference
- S-DP3.7 FDA UDI
- Description
- Depth Gauge FDA UDI
Identifiers
- Catalog Number
- S-DP3.7 FDA UDI
- Primary DI / UDI-DI
- 07640168190101 FDA UDI
- FDA Product Code
- NDP FDA UDI
- GMDN Term
- Surgical screwdriver, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3980 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
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
implantswiss by Novodent SA — 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
- Novodent SA
Sources (1)
- FDA UDI 55aad2ce-76d2-4f90-9f02-dfe91be74365 35 fields · synced May 30, 2026