eudamed_udi
Primary ID: 06430053261990
WOODCAST (UDI 06430053261990)
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 06430053261990
Device Regulatory Overview
The WOODCAST (Model/Catalog Number: C1480 Black) 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
- C1480 Black
- Product Code / EMDN
- M03050201
- Device Name
- WOODCAST 2mm
- 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 06430053261990.
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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