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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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CAVO ADATTATORE RF TIPO THERMEDICO NK1 — 3 UDI-DI variants, MDR

MD Atlas
NEURIMPULSE S.R.L.

Data from EUDAMED, last updated May 31, 2026

CAVO ADATTATORE RF TIPO THERMEDICO NK1

805367701AGOADA94

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: NEURIMPULSE S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805367701AGOADA94
Device name: CAVO ADATTATORE RF TIPO THERMEDICO NK1
Device model: ADATHER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: NEURIMPULSE S.R.L.
SRN: IT-MF-000016801
Country: Italy
Email: eudamed@neurimpulse.com
Phone: +39 049 635999

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KS5CRVP1R7W0SVS033H4VHBX

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

ADABAYL08053677017026
ADACOSM08053677017019
ADATHER08053677017033