GUDIDData
gudid Primary ID: 2532

AMSCO (UDI 2532)

Manufactured by Corporation Steris Canada

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AMSCO - Primary ID 2532

Device Regulatory Overview

The AMSCO (Model/Catalog Number: 2532) is a medical device manufactured by Corporation Steris Canada. This product is indexed under FDA Product Code / Category Classification MEC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2532
Product Code / EMDN
MEC
Device Name
The AMSCO 2532 Single-Chamber Washer Disinfector is intended for use in the cleaning and intermediate-level disinfection of soiled reusable utensils, trays, glassware, rubber and plastic goods, simple hard-surfaced rigid surgical instruments (such as forceps and clamps) and other similar items found in healthcare facilities.
Database Sync Date
2026-08-09 09:19:09

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 AMSCO?

The registered manufacturer of record for AMSCO is Corporation Steris Canada.

What is the Primary UDI-DI identifier for AMSCO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2532.

What classification code is assigned to this device?

This device is registered under product classification code MEC.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint