GUDIDData
eudamed_udi Primary ID: 08682503002419

AYSAM (UDI 08682503002419)

Manufactured by Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AYSAM - Primary ID 08682503002419

Device Regulatory Overview

The AYSAM (Model/Catalog Number: A520.13) is a medical device manufactured by Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi. This product is indexed under FDA Product Code / Category Classification S010499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
A520.13
Product Code / EMDN
S010499
Device Name
Sterilization Container Systems
Database Sync Date
2026-08-09 16:28:44

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 AYSAM?

The registered manufacturer of record for AYSAM is Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi.

What is the Primary UDI-DI identifier for AYSAM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682503002419.

What classification code is assigned to this device?

This device is registered under product classification code S010499.

Similar Classification Devices (S010499)

Other Devices by Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi

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