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Optimize

FDA UDI

Class I (US FDA UDI)

by Tdv Dental Ltda

Identity

Trade Name
OPTIMIZE FDA UDI
Generic Name
Dental abrasive disk, reusable FDA UDI
Device Name
Optimize Point Refill - 8 pieces + mandrel (EN/FR) FDA UDI
Model / Reference
0000000010 FDA UDI
Description
Optimize Point Refill - 8 pieces + mandrel (EN/FR) FDA UDI

Identifiers

Catalog Number
0000000010 FDA UDI
Primary DI / UDI-DI
07897990300066 FDA UDI
FDA Product Code
EHL FDA UDI
GMDN Term
Dental abrasive disk, 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental abrasive disk, reusable

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

Similar devices

Also classified as Dental abrasive disk, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tdv Dental Ltda

Sources (1)

  • FDA UDI 6750bb36-84c7-4cdf-8f21-0fd96f6fcf7b 35 fields · synced May 30, 2026