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Md 30

FDA UDI

Class II (US FDA UDI)

by Nouvag AG

Identity

Trade Name
MD 30 FDA UDI
Generic Name
Remotely-driven dental drilling system motor FDA UDI
Device Name
Dental implant motor system, SET FDA UDI
Model / Reference
2004 FDA UDI
Description
Dental implant motor system, SET FDA UDI

Identifiers

Primary DI / UDI-DI
ENOU20040 FDA UDI
510(k) Number
K042434 FDA UDI
FDA Product Code
DZI FDA UDI
GMDN Term
Remotely-driven dental drilling system motor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4120 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Remotely-driven dental drilling system motor

Md 30 by Nouvag AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Remotely-driven dental drilling system motor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nouvag AG

Sources (1)

  • FDA UDI 0fec0402-f33a-4758-864e-a6b0319fb674 35 fields · synced Jun 1, 2026