eudamed_udi
Primary ID: 06430053264908
WOODCAST (UDI 06430053264908)
Manufactured by Dassiet Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WOODCAST - Primary ID 06430053264908
Device Regulatory Overview
The WOODCAST (Model/Catalog Number: F1480S) is a medical device manufactured by Dassiet Oy. This product is indexed under FDA Product Code / Category Classification M03050201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F1480S
- Product Code / EMDN
- M03050201
- Device Name
- WOODCAST Soft
- Database Sync Date
- 2026-08-09 16:28:51
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 WOODCAST?
The registered manufacturer of record for WOODCAST is Dassiet Oy.
What is the Primary UDI-DI identifier for WOODCAST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430053264908.
What classification code is assigned to this device?
This device is registered under product classification code M03050201.
Similar Classification Devices (M03050201)
Other Devices by Dassiet Oy
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