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Protaper Gold Size Verifier

FDA UDI

Class I (US FDA UDI)

by Tulsa Dental Products Llc

Identity

Trade Name
Protaper Gold Size Verifier FDA UDI
Generic Name
Manual endodontic file/rasp, reusable FDA UDI
Device Name
ProTaper GOLD Size Verifier F2 FDA UDI
Model / Reference
PTGSVF2 FDA UDI
Description
ProTaper GOLD Size Verifier F2 FDA UDI

Identifiers

Catalog Number
PTGSVF2 FDA UDI
Primary DI / UDI-DI
D716PTGSVF21 FDA UDI
FDA Product Code
EIL FDA UDI
GMDN Term
Manual endodontic file/rasp, 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Manual endodontic file/rasp, reusable

Protaper Gold Size Verifier by Tulsa Dental Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual endodontic file/rasp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0ce7fd4f-7b93-4c80-aef9-a752a1e9a9c4 34 fields · synced May 30, 2026