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Endo 1500 Mid Medi

FDA UDI

Class II (US FDA UDI)

by Micro Mega

Identity

Trade Name
ENDO 1500 MID MEDI FDA UDI
Generic Name
Dental power tool system, pneumatic FDA UDI
Device Name
Dental handpiece for endontic treatment which works with Sonic vibtration FDA UDI
Model / Reference
MID FDA UDI
Description
Dental handpiece for endontic treatment which works with Sonic vibtration FDA UDI

Identifiers

Catalog Number
50400011 FDA UDI
Primary DI / UDI-DI
J015504000110 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Dental power tool system, pneumatic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4850 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

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental power tool system, pneumatic

Endo 1500 Mid Medi by Micro Mega — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental power tool system, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Micro Mega

Sources (1)

  • FDA UDI bd06e880-cf45-448b-acbb-7de9047024c6 34 fields · synced May 30, 2026