Reicodent

FDA UDI

Class I (US FDA UDI)

by devemed GmbH

Identity

Trade Name: Reicodent FDA UDI
Generic Name: Dental mirror, reusable FDA UDI
Device Name: Photo Mirror | 53/31 x 142 mm Rhodium FS - DoubleS lateral FDA UDI
Model / Reference: 02-2366-50 FDA UDI
Description: Photo Mirror | 53/31 x 142 mm Rhodium FS - DoubleS lateral FDA UDI

Identifiers

Primary DI / UDI-DI: 04061644061426 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

Yes

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

Reicodent by devemed GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental mirror, reusable.

MIRROR — KLS-Martin L.P. · Class I
TUCKER SCALER-B7-U15H — W.H. Holden, Inc. · Class I
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
Henry Schein — HENRY SCHEIN, INC. · 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: devemed GmbH

Sources (1)

FDA UDI 8ec0e15f-aa82-4f73-b879-1477695493d0 34 fields · synced Jun 1, 2026