Meijer

FDA UDI

Class I (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name: Meijer FDA UDI
Generic Name: Dental mirror, reusable FDA UDI
Device Name: Dental Tools FDA UDI
Model / Reference: SQY FDA UDI
Description: Dental Tools FDA UDI

Identifiers

Primary DI / UDI-DI: 00713733815628 FDA UDI
FDA Product Code: EAX FDA UDI
EMN FDA UDI
JET FDA UDI
GMDN Term: Dental mirror, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 FDA UDI
872.6650 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

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Manual dental scaler, reusable Dental mirror, reusable Periodontal pick/brush, reusable

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

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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: Meijer, Inc.

Sources (1)

FDA UDI 2791931f-883f-4c74-9b64-018dd9235b5c 33 fields · synced May 30, 2026