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Rotadent®

FDA UDI

Class I (US FDA UDI)

by Den-Mat Holdings, LLC

Identity

Trade Name
Rotadent® FDA UDI
Generic Name
Dental material application tool, single-use FDA UDI
Device Name
RD CLASSIC SHORT TIP BRSHD BLK FDA UDI
Model / Reference
9090S FDA UDI
Description
RD CLASSIC SHORT TIP BRSHD BLK FDA UDI

Identifiers

Catalog Number
9090S FDA UDI
Primary DI / UDI-DI
D8139090S0 FDA UDI
FDA Product Code
JEQ FDA UDI
GMDN Term
Dental material application tool, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6865 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental material application tool, single-use

Rotadent® by Den-Mat Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material application tool, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e6a93e5f-175a-4972-8177-6826b1501619 35 fields · synced Jun 9, 2026