GUDIDData
gudid Primary ID: 05.03.0002

PowerKnot High Strength Sutures (UDI 05.03.0002)

Manufactured by Medacta International SA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PowerKnot High Strength Sutures - Primary ID 05.03.0002

Device Regulatory Overview

The PowerKnot High Strength Sutures (Model/Catalog Number: 05.03.0002) is a medical device manufactured by Medacta International SA. This product is indexed under FDA Product Code / Category Classification GAT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
05.03.0002
Product Code / EMDN
GAT
Device Name
PowerKnot, #2, white/blue
Database Sync Date
2026-08-09 09:03:17

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 PowerKnot High Strength Sutures?

The registered manufacturer of record for PowerKnot High Strength Sutures is Medacta International SA.

What is the Primary UDI-DI identifier for PowerKnot High Strength Sutures?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05.03.0002.

What classification code is assigned to this device?

This device is registered under product classification code GAT.

Programmatic Export

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

JSON API Endpoint