← Back to catalogue

Medidenta

FDA UDI

Class I (US FDA UDI)

by Medidenta

Identity

Trade Name
Medidenta FDA UDI
Generic Name
Dental surgical power tool motorized handpiece/set, pneumatic FDA UDI
Device Name
Air Free Titan 90 Standard Head Highspeed Handpiece FDA UDI
Model / Reference
AFT90-PD FDA UDI
Description
Air Free Titan 90 Standard Head Highspeed Handpiece FDA UDI

Identifiers

Catalog Number
AFT90-PD FDA UDI
Primary DI / UDI-DI
00850046903243 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Dental surgical power tool motorized handpiece/set, pneumatic 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 surgical power tool motorized handpiece/set, pneumatic

Medidenta by Medidenta — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical power tool motorized handpiece/set, pneumatic.

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
Medidenta

Sources (1)

  • FDA UDI 1c1a3184-a4cc-4227-b89b-ba2f54cf84d2 34 fields · synced May 30, 2026