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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
Dressing/utility forceps, scissors-like, reusable FDA UDI
Device Name
ULTRASONIC INSERT CAVITRON 30KHZDF100/30K PERIO THIN UNIT POWER SETTING : LOW-MED INTERNAL WATER FLOW FDA UDI
Model / Reference
7611 FDA UDI
Description
ULTRASONIC INSERT CAVITRON 30KHZDF100/30K PERIO THIN UNIT POWER SETTING : LOW-MED INTERNAL WATER FLOW FDA UDI

Identifiers

Catalog Number
7611 FDA UDI
Primary DI / UDI-DI
D9437611 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Dressing/utility forceps, scissors-like, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e5eff01a-504c-469a-8729-45a96d3c39a6 36 fields · synced Jun 1, 2026