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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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medEctoin® Allergy Nasal Spray 1% /… — 5 UDI-DI variants, MDR

MD Atlas
bitop AG

Data from EUDAMED, last updated May 23, 2026

medEctoin® Allergy Nasal Spray 1% / medEctoin® Allergy Nasal Spray 2% / medEctoin® Rhinitis Nasal Spray

426026522ANS3KZG

5 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: bitop AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426026522ANS3KZG
Device name: medEctoin® Allergy Nasal Spray 1% / medEctoin® Allergy Nasal Spray 2% / medEctoin® Rhinitis Nasal Spray
Device model: ANS02/ANS03/ANS07
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: bitop AG
SRN: DE-MF-000006543
Country: Germany
Email: info@bitop.de

Variants by status

UDI-DI variants

5 UDI-DI variants

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basicUdiUlid01K2YSRZZB6FHJ213JW94SZNV3

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

3802404260265220018
3802104260265220094
3802504260265220001
3802604260265220025
3802204260265220100