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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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Adenoid curette — 21 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

Adenoid curette

403923900000069838

21 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: Aesculap AG

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 403923900000069838
Device name: Adenoid curette
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: Aesculap AG
SRN: DE-MF-000005504
Country: Germany
Email: eudamed@bbraun.com

Variants by status

UDI-DI variants

21 UDI-DI variants

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Applied filters

basicUdiUlid01K58P53QN6X2AWPZ74CSB12W7

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

Aesculap04038653179718
Aesculap04038653179633
Aesculap04038653179916
Aesculap04038653179688
Aesculap04038653179824
Aesculap04038653179701
Aesculap04038653179909
Aesculap04038653179862
Aesculap04038653179893
Aesculap04038653179671
Aesculap04038653179664
Aesculap04038653179848
Aesculap04038653179817
Aesculap04038653179640
Aesculap04038653179695
Aesculap04038653179886
Aesculap04038653179831
Aesculap04038653179657
Aesculap04038653179855
Aesculap04038653179725
Aesculap04038653179879