Identity
- Trade Name
- DS OmniTaper FDA UDI
- Generic Name
- Dental soft-tissue coring punch, single-use FDA UDI
- Device Name
- OmniTaper Mucosal Punch Ø3.4 GS FDA UDI
- Model / Reference
- 68017019 FDA UDI
- Description
- OmniTaper Mucosal Punch Ø3.4 GS FDA UDI
Identifiers
- Catalog Number
- 68017019 FDA UDI
- Primary DI / UDI-DI
- 07392532257599 FDA UDI
- FDA Product Code
- NDP FDA UDI
- GMDN Term
- Dental soft-tissue coring punch, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Commercial Distribution
- 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
No
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental soft-tissue coring punch, single-use
DS OmniTaper by Dentsply Implants Manufacturing GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental soft-tissue coring punch, single-use.
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- Punches, NOBEL — Omnia Spa · 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
- Dentsply Implants Manufacturing GmbH
Sources (1)
- FDA UDI b6f0ede2-cf60-4582-aecc-74ad75bfdec6 34 fields · synced May 29, 2026