eudamed_udi
Primary ID: D1231008100
ORINGER RETRACTOR (UDI D1231008100)
Manufactured by Dental Expert
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ORINGER RETRACTOR - Primary ID D1231008100
Device Regulatory Overview
The ORINGER RETRACTOR (Model/Catalog Number: 1008-10) is a medical device manufactured by Dental Expert. This product is indexed under FDA Product Code / Category Classification L150201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1008-10
- Product Code / EMDN
- L150201
- Device Name
- ORINGER RETRACTOR
- Database Sync Date
- 2026-08-09 16:45:07
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 ORINGER RETRACTOR?
The registered manufacturer of record for ORINGER RETRACTOR is Dental Expert.
What is the Primary UDI-DI identifier for ORINGER RETRACTOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D1231008100.
What classification code is assigned to this device?
This device is registered under product classification code L150201.
Similar Classification Devices (L150201)
Other Devices by Dental Expert
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