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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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Ultrasonic gel — 6 UDI-DI variants, MDR (Chemodis)

MD Atlas
Chemodis

Data from EUDAMED, last updated May 31, 2026

Ultrasonic gel

8715478ULTRASONIC8B

6 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: Chemodis

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8715478ULTRASONIC8B
Device name: Ultrasonic gel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: Chemodis
SRN: NL-MF-000023248
Country: Netherlands
Email: info@chemodis.nl
Phone: +31725205083

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JSRMEQEAB85YJQ0WBEWNM88W

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

8181108715478818119
8040108715478804013
8041508715478804150
8044508715478804457
8044108715478804419
8280108715478828019