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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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S-CAPEPLUS® Evacuation Mat - Basic Model — 1 UDI-DI variant, MDR

MD Atlas
Tetcon Global BV

Data from EUDAMED, last updated May 30, 2026

S-CAPEPLUS® Evacuation Mat - Basic Model

8720726730S-CAPEPLUSZT

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Tetcon Global BV

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8720726730S-CAPEPLUSZT
Device name: S-CAPEPLUS® Evacuation Mat - Basic Model
Device model: Basic Model
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: Tetcon Global BV
SRN: NL-MF-000029813
Country: Netherlands
Email: info@tetcon-ge.com
Phone: +31 40 298 99 55

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HS8FZ060JYCW24WQQN4WRXTS

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

S-CAPEPLUS® Basic Model08720726730044