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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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Medyz Swallowing Gel — 12 UDI-DI variants, MDR (Medyz BV)

MD Atlas
Medyz BV

Data from EUDAMED, last updated May 31, 2026

Medyz Swallowing Gel

087215166502SWALGELR2

12 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: Medyz BV

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UDI-DI variants

12 UDI-DI variants

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basicUdiUlid01KMQECHX13JKXA7TC0V80MH3J

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

Severo08721516650184
Severo08721516650221
Severo08721516650139
Severo08721516650207
Severo08721516650108
Severo08721516650160
SWAES08721516650320
SWAES08721516650368
SWAES08721516650245
SWAES08721516650344
SWAES08721516650276
SWAES08721516650306

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 087215166502SWALGELR2
Device name: Medyz Swallowing Gel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medyz BV
SRN: NL-MF-000051388
Country: Netherlands
Email: info@medyz.nl
Phone: +31629279030

Variants by status