GUDIDData
eudamed_udi Primary ID: 08904044201138

Knee Brace (Medio Lateral Stabiliser) Large (UDI 08904044201138)

Manufactured by Dynamic Techno Medicals Pvt Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Knee Brace (Medio Lateral Stabiliser) Large - Primary ID 08904044201138

Device Regulatory Overview

The Knee Brace (Medio Lateral Stabiliser) Large (Model/Catalog Number: 1271) is a medical device manufactured by Dynamic Techno Medicals Pvt Ltd. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1271
Product Code / EMDN
Y061209
Device Name
Dyna Knee Brace (Medio Lateral Stabiliser)
Database Sync Date
2026-08-09 16:46:40

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 Knee Brace (Medio Lateral Stabiliser) Large?

The registered manufacturer of record for Knee Brace (Medio Lateral Stabiliser) Large is Dynamic Techno Medicals Pvt Ltd.

What is the Primary UDI-DI identifier for Knee Brace (Medio Lateral Stabiliser) Large?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08904044201138.

What classification code is assigned to this device?

This device is registered under product classification code Y061209.

Programmatic Export

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

JSON API Endpoint