gudid Primary ID: 1

1000ML RECEPTAL CANISTER (UDI 1)

Manufactured by AMSINO INTERNATIONAL, INC.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The 1000ML RECEPTAL CANISTER (Model/Catalog Number: 1) is a medical device manufactured by AMSINO INTERNATIONAL, INC.. This product is indexed under FDA Product Code / Category Classification KDQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1
Product Code / EMDN: KDQ
Device Name: 1000ML RECEPTAL CANISTER
Database Sync Date: 2026-08-09 09:04:15

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 1000ML RECEPTAL CANISTER?

The registered manufacturer of record for 1000ML RECEPTAL CANISTER is AMSINO INTERNATIONAL, INC..

What is the Primary UDI-DI identifier for 1000ML RECEPTAL CANISTER?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.

What classification code is assigned to this device?

This device is registered under product classification code KDQ.

Similar Classification Devices (KDQ)

Other Devices by AMSINO INTERNATIONAL, INC.

Programmatic Export

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

JSON API Endpoint