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Power Dental USA

FDA UDI

Class I (US FDA UDI)

by Power Dental USA, Inc.

Identity

Trade Name
Power Dental USA FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
CASSETTES UTILITY PARTS BOX 80x30x25Hx0.7t, STAINLESS STEEL, FOR ULTRASONIC FDA UDI
Model / Reference
7533 FDA UDI
Description
CASSETTES UTILITY PARTS BOX 80x30x25Hx0.7t, STAINLESS STEEL, FOR ULTRASONIC FDA UDI

Identifiers

Catalog Number
7533 FDA UDI
Primary DI / UDI-DI
D94375330 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusableDevice sterilization/disinfection container, reusable

Power Dental USA by Power Dental USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI af3ecf44-7c1b-4d2a-b810-51f6650abe6e 35 fields · synced May 30, 2026