gudid Primary ID: SS-783-90 XL

Surtex (UDI SS-783-90 XL)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Surtex (Model/Catalog Number: SS-783-90 XL) is a medical device manufactured by SURTEX INSTRUMENTS LTD.. This product is indexed under FDA Product Code / Category Classification LRW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SS-783-90 XL
Product Code / EMDN: LRW
Device Name: Micro Vascular Scissors Round Handle - Delicate Blades - Angled 90 23 cm - 9" Stainless Steel
Database Sync Date: 2026-08-09 09:08:11

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 Surtex?

The registered manufacturer of record for Surtex is SURTEX INSTRUMENTS LTD..

What is the Primary UDI-DI identifier for Surtex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SS-783-90 XL.

What classification code is assigned to this device?

This device is registered under product classification code LRW.

Similar Classification Devices (LRW)

Other Devices by SURTEX INSTRUMENTS LTD.

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