eudamed_udi Primary ID: +M485AL1121206V0011S

ALTECH (UDI +M485AL1121206V0011S)

Manufactured by Meditera Tıbbi Malzeme Sanayi ve Ticaret A.Ş.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ALTECH (Model/Catalog Number: AL-1121-206.V001) is a medical device manufactured by Meditera Tıbbi Malzeme Sanayi ve Ticaret A.Ş.. This product is indexed under FDA Product Code / Category Classification R02010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AL-1121-206.V001
Product Code / EMDN: R02010102
Device Name: DOUBLE LINE/DOUBLE LUMEN BREATHING CIRCUIT (Non-Sterile)
Database Sync Date: 2026-08-09 16:47:27

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 ALTECH?

The registered manufacturer of record for ALTECH is Meditera Tıbbi Malzeme Sanayi ve Ticaret A.Ş..

What is the Primary UDI-DI identifier for ALTECH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +M485AL1121206V0011S.

What classification code is assigned to this device?

This device is registered under product classification code R02010102.

Similar Classification Devices (R02010102)

Other Devices by Meditera Tıbbi Malzeme Sanayi ve Ticaret A.Ş.

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