gudid
Primary ID: B2404200
Schick (UDI B2404200)
Manufactured by Dentsply International Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Schick - Primary ID B2404200
Device Regulatory Overview
The Schick (Model/Catalog Number: B2404200) is a medical device manufactured by Dentsply International Inc.. This product is indexed under FDA Product Code / Category Classification EHA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B2404200
- Product Code / EMDN
- EHA
- Device Name
- POSTERIOR AIMING RING
- 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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Get API Token Access ($49/mo)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 B2404200.
What classification code is assigned to this device?
This device is registered under product classification code EHA.
Similar Classification Devices (EHA)
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