gudid
Primary ID: 601-200
Intraoral Cheek Retractors (UDI 601-200)
Manufactured by ORTHO TECHNOLOGY, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Intraoral Cheek Retractors - Primary ID 601-200
Device Regulatory Overview
The Intraoral Cheek Retractors (Model/Catalog Number: 601-200) is a medical device manufactured by ORTHO TECHNOLOGY, INC.. This product is indexed under FDA Product Code / Category Classification EIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 601-200
- Product Code / EMDN
- EIF
- Device Name
- Retractor Intraoral HH Small Heat Sterilizable up to 370
- Database Sync Date
- 2026-08-09 09:00:47
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 Intraoral Cheek Retractors?
The registered manufacturer of record for Intraoral Cheek Retractors is ORTHO TECHNOLOGY, INC..
What is the Primary UDI-DI identifier for Intraoral Cheek Retractors?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 601-200.
What classification code is assigned to this device?
This device is registered under product classification code EIF.
Similar Classification Devices (EIF)
Other Devices by ORTHO TECHNOLOGY, INC.
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