eudamed_udi Primary ID: 08907536029807

SIORA (UDI 08907536029807)

Manufactured by SIORA SURGICALS PVT. LTD.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SIORA (Model/Catalog Number: Ti.131.106) is a medical device manufactured by SIORA SURGICALS PVT. LTD.. This product is indexed under FDA Product Code / Category Classification P09120503 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Ti.131.106
Product Code / EMDN: P09120503
Device Name: Quarter Tubular Plate-2.7mm, 6 Holes
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
}

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 SIORA?

The registered manufacturer of record for SIORA is SIORA SURGICALS PVT. LTD..

What is the Primary UDI-DI identifier for SIORA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08907536029807.

What classification code is assigned to this device?

This device is registered under product classification code P09120503.

Similar Classification Devices (P09120503)

Other Devices by SIORA SURGICALS PVT. LTD.

Programmatic Export

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

JSON API Endpoint