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Mectron

FDA UDI

Class II (US FDA UDI)

by Mectron Spa

Identity

Trade Name
MECTRON FDA UDI
Generic Name
Dental ultrasonic surgical system handpiece tip FDA UDI
Device Name
MT1204 is an osteotomy surgical insert to be used in conjunction with Mectron Piezosurgery handpieces FDA UDI
Model / Reference
MT1204 FDA UDI
Description
MT1204 is an osteotomy surgical insert to be used in conjunction with Mectron Piezosurgery handpieces FDA UDI

Identifiers

Catalog Number
03600019 FDA UDI
Primary DI / UDI-DI
E322036000190 FDA UDI
510(k) Number
K132848 FDA UDI
K153743 FDA UDI
FDA Product Code
JDX FDA UDI
DZI FDA UDI
ERL FDA UDI
HBE FDA UDI
HWE FDA UDI
GMDN Term
Dental ultrasonic surgical system handpiece tip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.4580 FDA UDI
872.4120 FDA UDI
874.4250 FDA UDI
882.4310 FDA UDI
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental ultrasonic surgical system handpiece tipHard-tissue ultrasonic surgical system handpiece tip

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

Similar devices

Also classified as Hard-tissue ultrasonic surgical system handpiece tip.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mectron Spa

Sources (1)

  • FDA UDI e094a9f8-7d8b-4871-858d-77a66faaa3a3 36 fields · synced May 30, 2026