← Back to catalogue

Mectron

FDA UDI

Class II (US FDA UDI)

by Mectron Spa

Identity

Trade Name
MECTRON FDA UDI
Generic Name
Dental ultrasonic surgical system handpiece FDA UDI
Device Name
Piezoelectric ultrasonic handpiece FDA UDI
Model / Reference
PIEZOSURGERY MT HANDPIECE FDA UDI
Description
Piezoelectric ultrasonic handpiece FDA UDI

Identifiers

Catalog Number
03120244 FDA UDI
Primary DI / UDI-DI
E322031202440 FDA UDI
510(k) Number
K242432 FDA UDI
FDA Product Code
ELC FDA UDI
DZI FDA UDI
GMDN Term
Dental ultrasonic surgical system handpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4850 FDA UDI
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: Dental ultrasonic surgical system handpiece

Mectron by Mectron Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental ultrasonic surgical system handpiece.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Mectron Spa

Sources (1)

  • FDA UDI ae42d574-1c64-4922-af91-81f5ef23b5e6 36 fields · synced Jun 1, 2026