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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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Nesty — 5 UDI-DI variants, MDR (conceptnatal)

MD Atlas
conceptnatal

Data from EUDAMED, last updated May 31, 2026

Nesty

42605981714NESTY5B

5 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: conceptnatal

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42605981714NESTY5B
Device name: Nesty
Device model: Textile cover for heated beds
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: conceptnatal
SRN: DE-MF-000010321
Country: Germany
Email: info@conceptnatal.de
Phone: +49 (0) 7127 9802601

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KSAMFVJ3BEJTVP1KKVNB1A6D

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

Nesty04260598171414
Nesty04260598171407
Nesty Twins04260598171469
Nesty Twins04260598171476
NestyFlex04260598171452