eudamed_udi
Primary ID: 14562185395522
CL AIA-PACK SAMPLE DILUTING REAGENT B (UDI 14562185395522)
Manufactured by Tosoh Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CL AIA-PACK SAMPLE DILUTING REAGENT B - Primary ID 14562185395522
Device Regulatory Overview
The CL AIA-PACK SAMPLE DILUTING REAGENT B (Model/Catalog Number: 0029402) is a medical device manufactured by Tosoh Corporation. This product is indexed under FDA Product Code / Category Classification W01029003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0029402
- Product Code / EMDN
- W01029003
- Device Name
- CL AIA-PACK SAMPLE DILUTING REAGENT B
- Database Sync Date
- 2026-08-09 16:48:48
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 CL AIA-PACK SAMPLE DILUTING REAGENT B?
The registered manufacturer of record for CL AIA-PACK SAMPLE DILUTING REAGENT B is Tosoh Corporation.
What is the Primary UDI-DI identifier for CL AIA-PACK SAMPLE DILUTING REAGENT B?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 14562185395522.
What classification code is assigned to this device?
This device is registered under product classification code W01029003.
Similar Classification Devices (W01029003)
Other Devices by Tosoh Corporation
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