eudamed_udi
Primary ID: 00724995226480
AMSCO (UDI 00724995226480)
Manufactured by STERIS Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AMSCO - Primary ID 00724995226480
Device Regulatory Overview
The AMSCO (Model/Catalog Number: EF3102352021010003) is a medical device manufactured by STERIS Corporation. This product is indexed under FDA Product Code / Category Classification Z12011304 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EF3102352021010003
- Product Code / EMDN
- Z12011304
- Device Name
- AMSCO 600 Steam Sterilizer
- Database Sync Date
- 2026-08-09 16:45:59
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 AMSCO?
The registered manufacturer of record for AMSCO is STERIS Corporation.
What is the Primary UDI-DI identifier for AMSCO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00724995226480.
What classification code is assigned to this device?
This device is registered under product classification code Z12011304.
Similar Classification Devices (Z12011304)
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