eudamed_udi
Primary ID: M294L1701020
Ocular and endocular retractors, reusable (UDI M294L1701020)
Manufactured by CLINIMED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ocular and endocular retractors, reusable - Primary ID M294L1701020
Device Regulatory Overview
The Ocular and endocular retractors, reusable (Model/Catalog Number: L170102) is a medical device manufactured by CLINIMED. This product is indexed under FDA Product Code / Category Classification L170102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- L170102
- Product Code / EMDN
- L170102
- Device Name
- Ocular and endocular retractors, reusable
- Database Sync Date
- 2026-08-09 16:48:58
Full Regulatory Attributes
🔒 Token Gated
{
"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 Ocular and endocular retractors, reusable?
The registered manufacturer of record for Ocular and endocular retractors, reusable is CLINIMED.
What is the Primary UDI-DI identifier for Ocular and endocular retractors, reusable?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M294L1701020.
What classification code is assigned to this device?
This device is registered under product classification code L170102.
Similar Classification Devices (L170102)
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