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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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Laryngoscope — 8 UDI-DI variants, MDR (Henke-Sass, Wolf GmbH)

MD Atlas
Henke-Sass, Wolf GmbH

Data from EUDAMED, last updated May 23, 2026

Laryngoscope

4035873120101039U

8 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: Henke-Sass, Wolf GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4035873120101039U
Device name: Laryngoscope
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 2, 2026

Manufacturer & authorised representative

Manufacturer

Name: Henke-Sass, Wolf GmbH
SRN: DE-MF-000005531
Country: Germany
Email: andreas.mantay@henkesasswolf.de
Phone: 074629466473

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KGEQ5Y0TWDEW0DK9A8ZN46E3

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

LARYN 6/70° 159 AK HM HSW04035873064169
Laryngoscope04035873070214
Laryngoscope04035873064176
Laryngoscopes04035873070832
LARYNGOSCOPES04035873011194
LARYNGOSCOPES04035873011170
LARYNGOSCOPES04035873063650
LARYNGOSCOPES04035873070849