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Diaprophy

FDA UDI

Class I (US FDA UDI)

by Diaswiss SA

Identity

Trade Name
Diaprophy FDA UDI
Generic Name
Dental abrasive point, reusable FDA UDI
Device Name
Dental rotary polishing instrument for intraoral use FDA UDI
Model / Reference
271UM-0 FDA UDI
Description
Dental rotary polishing instrument for intraoral use FDA UDI

Identifiers

Primary DI / UDI-DI
07630049985162 FDA UDI
FDA Product Code
EHL FDA UDI
GMDN Term
Dental abrasive point, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6010 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental abrasive point, reusable

Diaprophy by Diaswiss SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental abrasive point, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diaswiss SA

Sources (1)

  • FDA UDI 08bb2d2e-ee59-44f8-b4e0-d94c83617a25 33 fields · synced Jun 1, 2026