eudamed_udi
Primary ID: 04560189211186
Unspecified Brand (UDI 04560189211186)
Manufactured by Tosoh Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 04560189211186
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 0020359) is a medical device manufactured by Tosoh Corporation. This product is indexed under FDA Product Code / Category Classification W0102039002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0020359
- Product Code / EMDN
- W0102039002
- Device Name
- AIA-PACK BMG CALIBRATOR SET
- Database Sync Date
- 2026-08-09 17:35:19
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Tosoh Corporation.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04560189211186.
What classification code is assigned to this device?
This device is registered under product classification code W0102039002.
Similar Classification Devices (W0102039002)
Other Devices by Tosoh Corporation
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint