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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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IncoGlide — 9 UDI-DI variants, MDR (DecoCare)

MD Atlas
DecoCare

Data from EUDAMED, last updated May 30, 2026

IncoGlide

87209382653211XZ

9 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: DecoCare

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87209382653211XZ
Device name: IncoGlide
Device model: 3211 (100 x 140 cm)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 15, 2023

Manufacturer & authorised representative

Manufacturer

Name: DecoCare
SRN: NL-MF-000015695
Country: Netherlands
Email: m.kluitmans@decocare.nl

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01GVJ8FSX3SHDBRZ4SQDSXT85X

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

953308720938265327
953208720938265310
225708720938265297
953708720938265358
953808720938265365
953608720938265341
321008720938265488
IncoGlide08720938265044
IncoGlide08720938265280