GUDIDData
eudamed_udi Primary ID: 08682503006585

Aysam (UDI 08682503006585)

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 08682503006585

Device Regulatory Overview

The Aysam (Model/Catalog Number: AH908MFSBO0XS) 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 P09088007 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AH908MFSBO0XS
Product Code / EMDN
P09088007
Device Name
FEMORAL GÖVDE- STEM BAĞLANTI CİVATASI XS/FEMORAL BODY-STEM FASTENER BOLT XS
Database Sync Date
2026-08-09 16:51:48

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 08682503006585.

What classification code is assigned to this device?

This device is registered under product classification code P09088007.

Similar Classification Devices (P09088007)

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

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