← Back to catalogue

Ti-Max X

FDA UDI

Class II (US FDA UDI)

by Nakanishi Inc.

Identity

Trade Name
Ti-Max X FDA UDI
Generic Name
Dental surgical power tool motorized handpiece/set, electric FDA UDI
Model / Reference
X-SG65L FDA UDI

Identifiers

Primary DI / UDI-DI
04560264560529 FDA UDI
FDA Product Code
KMW FDA UDI
GMDN Term
Dental surgical power tool motorized handpiece/set, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental surgical power tool motorized handpiece/set, electric

Ti-Max X by Nakanishi Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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
Nakanishi Inc.

Sources (1)

  • FDA UDI 6b5aa49d-f1dc-4787-a5b0-7e9b9db8b93f 32 fields · synced May 31, 2026