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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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Nasal Aspirator — 5 UDI-DI variants, MDR

MD Atlas
Albert Hohlkörper GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Nasal Aspirator

40375664000MF

5 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: Albert Hohlkörper GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40375664000MF
Device name: Nasal Aspirator
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 4, 2023

Manufacturer & authorised representative

Manufacturer

Name: Albert Hohlkörper GmbH & Co. KG
SRN: DE-MF-000005482
Country: Germany
Email: info@albert.de
Phone: ++49 (0) 2372 92720

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01GNY9ZFZK695GCBNF64T8JRPY

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

Poire à oreilles 41ml04037566001550
P200.2.1000104037566001185
B000404037566001420
1025606504037566001833
P250.3.30001+Z288.3204037566001611