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Diamond Strip

FDA UDI

Class I (US FDA UDI)

by Tdv Dental Ltda

Identity

Trade Name
DIAMOND STRIP FDA UDI
Generic Name
Dental abrasive strip, single-use FDA UDI
Device Name
Diamond Strip 2.5 mm - 12 Units (EN/FR) FDA UDI
Model / Reference
0006010001 FDA UDI
Description
Diamond Strip 2.5 mm - 12 Units (EN/FR) FDA UDI

Identifiers

Catalog Number
0006010001 FDA UDI
Primary DI / UDI-DI
07897990302398 FDA UDI
FDA Product Code
EHM FDA UDI
GMDN Term
Dental abrasive strip, 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 strip, single-use

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

Similar devices

Also classified as Dental abrasive strip, single-use.

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 8a65e640-1f19-4e0a-a608-4fcde52f7233 34 fields · synced May 30, 2026