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Prophy Rubber Cup

FDA UDI

Class I (US FDA UDI)

by DiaDent Group International

Identity

Trade Name
Prophy Rubber Cup FDA UDI
Generic Name
Dental-professional prophylaxis brush, single-use FDA UDI
Device Name
A rotational device, typically made from rubber material, that is used to apply polishing agents during dental prophylaxis (cleaning). FDA UDI
Model / Reference
Ribbed, Snap-On FDA UDI
Description
A rotational device, typically made from rubber material, that is used to apply polishing agents during dental prophylaxis (cleaning). FDA UDI

Identifiers

Catalog Number
950-251 FDA UDI
Primary DI / UDI-DI
08806383525886 FDA UDI
FDA Product Code
EHK FDA UDI
GMDN Term
Dental-professional prophylaxis brush, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6290 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental polishing cup, single-useDental-professional prophylaxis brush, single-use

Prophy Rubber Cup by DiaDent Group International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental-professional prophylaxis brush, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1e5e4664-5e39-4957-b764-c984f96ff3ac 35 fields · synced Jun 6, 2026