Lasi-Kostamo Lasi-imukärki (AR-lasi) Ø 1,5 mm pituus 11 cm pakkauksessa 50 (UDI 06430071660171)
Manufactured by Lasi-Kostamo Oy
Device Regulatory Overview
The Lasi-Kostamo Lasi-imukärki (AR-lasi) Ø 1,5 mm pituus 11 cm pakkauksessa 50 (Model/Catalog Number: LaKo/imk 1,5/11) 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 1,5/11
- Product Code / EMDN
- A0680
- Device Name
- Lasi-Kostamo Lasi-imukärki (AR-lasi)
- Database Sync Date
- 2026-08-09 16:48:44
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 Lasi-Kostamo Lasi-imukärki (AR-lasi) Ø 1,5 mm pituus 11 cm pakkauksessa 50?
The registered manufacturer of record for Lasi-Kostamo Lasi-imukärki (AR-lasi) Ø 1,5 mm pituus 11 cm pakkauksessa 50 is Lasi-Kostamo Oy.
What is the Primary UDI-DI identifier for Lasi-Kostamo Lasi-imukärki (AR-lasi) Ø 1,5 mm pituus 11 cm pakkauksessa 50?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430071660171.
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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