Schick (UDI B1218052)

Manufactured by Dentsply International Inc.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Schick (Model/Catalog Number: B1218052) is a medical device manufactured by Dentsply International Inc.. This product is indexed under FDA Product Code / Category Classification MQB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: B1218052
Product Code / EMDN: MQB
Device Name: SCHICK33 S2 SENSOR RMA KIT, 9FT
Database Sync Date: 2026-08-09 09:02:02

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Schick?

The registered manufacturer of record for Schick is Dentsply International Inc..

What is the Primary UDI-DI identifier for Schick?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B1218052.

What classification code is assigned to this device?

This device is registered under product classification code MQB.

Similar Classification Devices (MQB)

Other Devices by Dentsply International Inc.

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