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Fibrapost Plus N°2

FDA UDI

Class I (US FDA UDI)

by Produits dentaires S.A.

Identity

Trade Name
FIBRAPOST PLUS N°2 FDA UDI
Generic Name
Root canal post, preformed FDA UDI
Device Name
Glass fibre posts - Core build up - Rack of 12 Total Length 19mm Length of tapered part 11mm Diameter of the lower tip 1.06mm Diameter of the cylindrical part 1.50mm FDA UDI
Model / Reference
22597 FDA UDI
Description
Glass fibre posts - Core build up - Rack of 12 Total Length 19mm Length of tapered part 11mm Diameter of the lower tip 1.06mm Diameter of the cylindrical part 1.50mm FDA UDI

Identifiers

Primary DI / UDI-DI
07640159162902 FDA UDI
FDA Product Code
ELR FDA UDI
GMDN Term
Root canal post, preformed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3810 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

Yes

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

Category: Root canal post, preformed

Fibrapost Plus N°2 by Produits dentaires S.A. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Root canal post, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d2188349-46a3-4236-b525-dc5f7a159236 34 fields · synced May 30, 2026