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ProTaper Ultimate Conform Fit

FDA UDI

Class I (US FDA UDI)

by Tulsa Dental Products Llc

Identity

Trade Name
ProTaper Ultimate Conform Fit FDA UDI
Generic Name
Synthetic gutta-percha FDA UDI
Device Name
ProTaper Ultimate Conform Fit Gutta-Percha Points Size F2 FDA UDI
Model / Reference
PULGF2 FDA UDI
Description
ProTaper Ultimate Conform Fit Gutta-Percha Points Size F2 FDA UDI

Identifiers

Catalog Number
PULGF2 FDA UDI
Primary DI / UDI-DI
D716PULGF21 FDA UDI
FDA Product Code
EKM FDA UDI
GMDN Term
Synthetic gutta-percha FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3850 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

Yes

FDA UDI

Category: Synthetic gutta-percha

ProTaper Ultimate Conform Fit by Tulsa Dental Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic gutta-percha.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c0dc2d3d-5258-4514-b696-f8e7c71d23c5 36 fields · synced Jun 1, 2026