← Back to catalogue

Fotoplus

FDA UDI

Class I (US FDA UDI)

by Tdv Dental Ltda

Identity

Trade Name
FOTOPLUS FDA UDI
Generic Name
Dental spatula, reusable FDA UDI
Device Name
Fotoplus - 2 Instruments (PT/ES/EN/FR) FDA UDI
Model / Reference
0005010000 FDA UDI
Description
Fotoplus - 2 Instruments (PT/ES/EN/FR) FDA UDI

Identifiers

Catalog Number
0005010000 FDA UDI
Primary DI / UDI-DI
07897990342011 FDA UDI
FDA Product Code
EIY FDA UDI
GMDN Term
Dental spatula, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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 spatula, reusable

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

Similar devices

Also classified as Dental spatula, reusable.

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 1cb71b87-dccd-4818-93cd-7e18f607739b 34 fields · synced Jun 1, 2026