GUDIDData
eudamed_udi Primary ID: 08594206966168

Plášť operační STANDARD CLASSIC sv. modrá/sv. modrá vel. MTM (UDI 08594206966168)

Manufactured by CLINITEX s.r.o.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Plášť operační STANDARD CLASSIC sv. modrá/sv. modrá vel. MTM - Primary ID 08594206966168

Device Regulatory Overview

The Plášť operační STANDARD CLASSIC sv. modrá/sv. modrá vel. MTM (Model/Catalog Number: N16BAAA1KDUHAHA00MTM) is a medical device manufactured by CLINITEX s.r.o.. This product is indexed under FDA Product Code / Category Classification T020401 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
N16BAAA1KDUHAHA00MTM
Product Code / EMDN
T020401
Device Name
Plášť operační STANDARD
Database Sync Date
2026-08-09 16:29:05

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 Plášť operační STANDARD CLASSIC sv. modrá/sv. modrá vel. MTM?

The registered manufacturer of record for Plášť operační STANDARD CLASSIC sv. modrá/sv. modrá vel. MTM is CLINITEX s.r.o..

What is the Primary UDI-DI identifier for Plášť operační STANDARD CLASSIC sv. modrá/sv. modrá vel. MTM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594206966168.

What classification code is assigned to this device?

This device is registered under product classification code T020401.

Programmatic Export

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

JSON API Endpoint