Henry Schein

FDA UDI

Class I (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name: Henry Schein FDA UDI
Generic Name: Dental mirror, reusable FDA UDI
Device Name: Mirror Fiberglass FS FDA UDI
Model / Reference: 1005067 FDA UDI
Description: Mirror Fiberglass FS FDA UDI

Identifiers

Catalog Number: 1005067 FDA UDI
Primary DI / UDI-DI: 00304040045510 FDA UDI
FDA Product Code: EAX FDA UDI
GMDN Term: Dental mirror, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

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

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental mirror, reusable

Henry Schein by Henry Schein, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental mirror, reusable.

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MOUTH MIRROR HANDLE, CONE SOCKET, HANDFORM, STAINLESS STEEL — W.H. Holden, Inc. · Class I
ZOLL-DENTAL — Zoll-Dental · Class I
Riofoto™ Mirrors — Ortho Organizers, Inc. · Class I
MIRROR — KLS-Martin L.P. · Class I
Plasdent — PLASDENT CORP. · Class I
Hahnenkratt — E. Hahnenkratt GmbH · 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: Henry Schein, Inc.

Sources (1)

FDA UDI 0c2a6cda-b37a-4e90-859b-1c1e2807de5a 34 fields · synced May 30, 2026