GUDIDData
eudamed_udi Primary ID: 07350052860736

Nima Köksdyna 39x36x10 cm (UDI 07350052860736)

Manufactured by Nimacare AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nima Köksdyna 39x36x10 cm - Primary ID 07350052860736

Device Regulatory Overview

The Nima Köksdyna 39x36x10 cm (Model/Catalog Number: DKH393610) is a medical device manufactured by Nimacare AB. This product is indexed under FDA Product Code / Category Classification V080399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DKH393610
Product Code / EMDN
V080399
Device Name
Nima Köksdyna
Database Sync Date
2026-08-09 16:28:46

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Nima Köksdyna 39x36x10 cm?

The registered manufacturer of record for Nima Köksdyna 39x36x10 cm is Nimacare AB.

What is the Primary UDI-DI identifier for Nima Köksdyna 39x36x10 cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350052860736.

What classification code is assigned to this device?

This device is registered under product classification code V080399.

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