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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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NEO 900 Foot Switch — 2 UDI-DI variants, MDR (Haag-Streit AG)

MD Atlas
Haag-Streit AG

Data from EUDAMED, last updated May 23, 2026

NEO 900 Foot Switch

764013298NEO900_Switch7S

2 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: Haag-Streit AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 764013298NEO900_Switch7S
Device name: NEO 900 Foot Switch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2023

Manufacturer & authorised representative

Manufacturer

Name: Haag-Streit AG
SRN: CH-MF-000020981
Country: Switzerland
Email: regulatory@haag-streit.com
Phone: +41 31 978 01 11

Authorised representative

Name: Haag-Streit Deutschland GmbH
SRN: DE-AR-000025462
Country: Germany
Phone: +49 4103 709 02

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H11EHS1SE3S7Y8MJFBY665VW

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

Foot Switch EF 500007640132987928
Foot Switch EF 500107640132988048