GUDIDData
gudid Primary ID: S3A

S3A (UDI S3A)

Manufactured by Aei Technologies, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for S3A - Primary ID S3A

Device Regulatory Overview

The S3A (Model/Catalog Number: S3A) is a medical device manufactured by Aei Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification CCL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
S3A
Product Code / EMDN
CCL
Device Name
Oxygen Analyzer
Database Sync Date
2026-08-09 09:06:20

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of S3A?

The registered manufacturer of record for S3A is Aei Technologies, Inc..

What is the Primary UDI-DI identifier for S3A?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S3A.

What classification code is assigned to this device?

This device is registered under product classification code CCL.

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