Mirafit White Glass Fiber Post Stnd. Kit(18) Asst. L2, L3, L4, Anterior

FDA UDI

Class I (US FDA UDI)

by Hager Worldwide, Inc.

Identity

Trade Name: MIRAFIT WHITE GLASS FIBER POST STND. KIT(18) ASST. L2, L3, L4, ANTERIOR FDA UDI
Generic Name: Root canal post, preformed FDA UDI
Device Name: Dental post FDA UDI
Model / Reference: 356044 FDA UDI
Description: Dental post FDA UDI

Identifiers

Primary DI / UDI-DI: D2483560441 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 Glass Fiber Post Stnd. Kit(18) Asst. L2, L3, L4, Anterior by Hager Worldwide, Inc. — Class I — FDA UDI — listed in FDA GUDID

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Also classified as Root canal post, preformed.

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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 11bb27fa-8932-435a-9781-675f0bc84d0d 34 fields · synced Jun 9, 2026