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DOTT DRY EYES Eye Drops - EUDAMED Registration 06251151002847

Access comprehensive regulatory information for DOTT DRY EYES Eye Drops in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 06251151002847 and manufactured by Amman Pharmaceutical Industries in Jordan.

This page provides complete registration details including trade name (DOTT DRY EYES Eye Drops), manufacturer information, authorized representative details, competent authority (Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.

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EUDAMED Official Data
Class IIa
06251151002847
No
DOTT DRY EYES Eye Drops
Trade Name: DOTT DRY EYES Eye Drops
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Device Description (EMDN)

OPHTHALMIC DEVICES - OTHER

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
Q0299
Trade Name
DOTT DRY EYES Eye Drops
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06251151002847
Basic UDI
6251151Q029-002PE
Version Date
December 05, 2024
Manufacturer Last Update
December 20, 2022
Active Status
No
Manufacturer
Country
Jordan
Country Type
NON_EU
Address
A3 Sahab AMMAN
Email
dania@ammanpharma.com
Authorized Representative
SRN
BE-AR-000011902
Country
Belgium
Address
Guldenberg 1 Map box 2-4 Antwerpen
Email
eurep@easymedicaldevice.com
Telephone
+32 484 39 01 11
Regulatory Information
Competent Authority
Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Spain
Market Available
Germany:None~None, Poland:None~None, Romania:None~None, Spain:2026-01-30~None
Device Characteristics
Human Tissues
No
Animal Tissues
No