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Power Dental USA

FDA UDI

Class II (US FDA UDI)

by Power Dental USA, Inc.

Identity

Trade Name
Power Dental USA FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
Device Name
SURGICAL SUCTION TUBE 3.0mm FDA UDI
Model / Reference
6742 FDA UDI
Description
SURGICAL SUCTION TUBE 3.0mm FDA UDI

Identifiers

Catalog Number
6742 FDA UDI
Primary DI / UDI-DI
D94367420 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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: Surgical/emergency suction cannula, non-illuminating, reusableDental suction system

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

Similar devices

Also classified as Dental suction system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7100dbef-98ad-4e41-89cd-0ec12b831c57 35 fields · synced May 30, 2026