eudamed_udi
Primary ID: 06430057230695
Suihkutuoli Anni EXW, muunneltava (UDI 06430057230695)
Manufactured by Tukimet Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Suihkutuoli Anni EXW, muunneltava - Primary ID 06430057230695
Device Regulatory Overview
The Suihkutuoli Anni EXW, muunneltava (Model/Catalog Number: 337610W) is a medical device manufactured by Tukimet Oy. This product is indexed under FDA Product Code / Category Classification Y180999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 337610W
- Product Code / EMDN
- Y180999
- Device Name
- Hygienia-apuväline
- Database Sync Date
- 2026-08-09 17:12:28
Full Regulatory Attributes
đź”’ 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 Suihkutuoli Anni EXW, muunneltava?
The registered manufacturer of record for Suihkutuoli Anni EXW, muunneltava is Tukimet Oy.
What is the Primary UDI-DI identifier for Suihkutuoli Anni EXW, muunneltava?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430057230695.
What classification code is assigned to this device?
This device is registered under product classification code Y180999.
Similar Classification Devices (Y180999)
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