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Medidenta

FDA UDI

Class I (US FDA UDI)

by Handpiece Parts & Repairs, Inc.

Identity

Trade Name
MEDIDENTA FDA UDI
Generic Name
Dental power tool system handpiece, line-powered FDA UDI
Device Name
MEDILECTRIC ELECTRIC HANDPIECE SYSTEM FDA UDI
Model / Reference
EJ0008-MEDI FDA UDI
Description
MEDILECTRIC ELECTRIC HANDPIECE SYSTEM FDA UDI

Identifiers

Catalog Number
EJ0008-MEDI FDA UDI
Primary DI / UDI-DI
00810988030377 FDA UDI
FDA Product Code
EBW FDA UDI
GMDN Term
Dental power tool system handpiece, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental power tool system handpiece, line-powered

Medidenta by Handpiece Parts & Repairs, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental power tool system handpiece, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Handpiece Parts & Repairs, Inc.

Sources (1)

  • FDA UDI 17e249b0-e5c6-41ec-bf36-9c096a394114 34 fields · synced Jun 8, 2026