← Back to catalogue

Sandpaper Discs

FDA UDI

Class I (US FDA UDI)

by Tdv Dental Ltda

Identity

Trade Name
SANDPAPER DISCS FDA UDI
Generic Name
Dental abrasive disk, single-use FDA UDI
Device Name
Sandpaper Discs 19mm - 100 assorted discs (EN/FR) FDA UDI
Model / Reference
0002020043 FDA UDI
Description
Sandpaper Discs 19mm - 100 assorted discs (EN/FR) FDA UDI

Identifiers

Catalog Number
0002020043 FDA UDI
Primary DI / UDI-DI
07897990301506 FDA UDI
FDA Product Code
EHJ FDA UDI
GMDN Term
Dental abrasive disk, single-use 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental abrasive disk, single-use

Sandpaper Discs by Tdv Dental Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental abrasive disk, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tdv Dental Ltda

Sources (1)

  • FDA UDI da7dbf70-a4ba-4f82-ad3b-0151554ae1ce 35 fields · synced May 30, 2026