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Microprophy

FDA UDI

Class I (US FDA UDI)

by Danville Materials, Llc

Identity

Trade Name
MICROPROPHY FDA UDI
Generic Name
Dental polishing brush FDA UDI
Device Name
MICROPROPHY II FDA UDI
Model / Reference
201684-00 FDA UDI
Description
MICROPROPHY II FDA UDI

Identifiers

Catalog Number
201684-00 FDA UDI
Primary DI / UDI-DI
00816594021624 FDA UDI
FDA Product Code
EJR FDA UDI
GMDN Term
Dental polishing brush FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6030 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

Yes

FDA UDI

Lot / Batch Number

Yes

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: Dental polishing brush

Microprophy by Danville Materials, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental polishing brush.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 97389920-5b00-466a-ad63-d947e672554c 35 fields · synced May 30, 2026