eudamed_udi Primary ID: 06430071660195

Lasi-Kostamo Lasi-imukärki (AR-lasi) Ø 1,5 mm pituus 6 cm pakkauksessa 100 (UDI 06430071660195)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lasi-Kostamo Lasi-imukärki (AR-lasi) Ø 1,5 mm pituus 6 cm pakkauksessa 100 (Model/Catalog Number: LaKo/imk 1,5/6) is a medical device manufactured by Lasi-Kostamo Oy. This product is indexed under FDA Product Code / Category Classification A0680 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: LaKo/imk 1,5/6
Product Code / EMDN: A0680
Device Name: Lasi-Kostamo Lasi-imukärki (AR-lasi)
Database Sync Date: 2026-08-09 16:48:07

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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Frequently Asked Questions

Who is the primary manufacturer of Lasi-Kostamo Lasi-imukärki (AR-lasi) Ø 1,5 mm pituus 6 cm pakkauksessa 100?

The registered manufacturer of record for Lasi-Kostamo Lasi-imukärki (AR-lasi) Ø 1,5 mm pituus 6 cm pakkauksessa 100 is Lasi-Kostamo Oy.

What is the Primary UDI-DI identifier for Lasi-Kostamo Lasi-imukärki (AR-lasi) Ø 1,5 mm pituus 6 cm pakkauksessa 100?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430071660195.

What classification code is assigned to this device?

This device is registered under product classification code A0680.

Similar Classification Devices (A0680)

Other Devices by Lasi-Kostamo Oy

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