gudid Primary ID: BAS KOL 115V/60Hz 3bar NO

DK50 DS (UDI BAS KOL 115V/60Hz 3bar NO)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DK50 DS (Model/Catalog Number: BAS KOL 115V/60Hz 3bar NO) is a medical device manufactured by EKOM spol. s r.o.. This product is indexed under FDA Product Code / Category Classification BTI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: BAS KOL 115V/60Hz 3bar NO
Product Code / EMDN: BTI
Device Name
Database Sync Date: 2026-08-09 09:41:10

Full Regulatory Attributes

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{
    "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 DK50 DS?

The registered manufacturer of record for DK50 DS is EKOM spol. s r.o..

What is the Primary UDI-DI identifier for DK50 DS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BAS KOL 115V/60Hz 3bar NO.

What classification code is assigned to this device?

This device is registered under product classification code BTI.

Similar Classification Devices (BTI)

Other Devices by EKOM spol. s r.o.

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