eudamed_udi
Primary ID: 04560189211407
Unspecified Brand (UDI 04560189211407)
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 04560189211407
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 0020360) is a medical device manufactured by Tosoh Corporation. This product is indexed under FDA Product Code / Category Classification W0102060103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0020360
- Product Code / EMDN
- W0102060103
- Device Name
- AIA-PACK IRI CALIBRATOR SET
- Database Sync Date
- 2026-08-09 17:26:14
Full Regulatory Attributes
π 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 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 04560189211407.
What classification code is assigned to this device?
This device is registered under product classification code W0102060103.
Similar Classification Devices (W0102060103)
Other Devices by Tosoh Corporation
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