Mirafit White - Starter Kit (18)assorted

FDA UDI

Class I (US FDA UDI)

by Hager Worldwide, Inc.

Identity

Trade Name: MIRAFIT WHITE - STARTER KIT (18)ASSORTED FDA UDI
Generic Name: Root canal post, preformed FDA UDI
Device Name: Dental post reamer FDA UDI
Model / Reference: 356059 FDA UDI
Description: Dental post reamer FDA UDI

Identifiers

Primary DI / UDI-DI: D2483560591 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Root canal post, preformed

Mirafit White - Starter Kit (18)assorted by Hager Worldwide, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Root canal post, preformed.

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FIBRAPOST PLUS N°1-4 (24 glass fibre posts + 4 reamers + 1 screwdiver) — Produits dentaires S.A. · Class I
MACRO-LOCK OVAL INTRO KIT A — RECHERCHES TECHNIQUES DENTAIRES · Class I
Flexi-Overdenture — ESSENTIAL DENTAL SYSTEMS, INC. · Class I
FibreKleer 4x — KERR CORPORATION · Class I
BENCO — BENCO DENTAL SUPPLY CO. · Class I
Darby Dental Supply, LLC — DARBY DENTAL SUPPLY, LLC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Hager Worldwide, Inc.

Sources (1)

FDA UDI 2ef66a7e-5636-4d4d-a7f0-4a019e17763e 34 fields · synced Jun 9, 2026