A device withdrawn or recalled? You see it before anyone else.
If a device you supply changes status in the EU register — withdrawn, recalled — you're alerted, without having to check yourself. No more manual monitoring.
Scan a box's DataMatrix and see it instantly — risk class, manufacturer, certificate, user manual. The very same scan your customers use to pull up their own manual.
MD Atlas brings the device checks your regulations require — and the answers your customers keep asking for — right to your counter.
Device
Central venous catheter
UDI-DI · 03512345678906
[ Mockup — MD Atlas scanner preview ]
MDR Article 14 makes every pharmacy that supplies a CE-marked device a distributor: you must verify the CE marking, certificate and UDI before handing it over, keep a record, and act on recalls.
The same duty applies in every EU member state. And now that EUDAMED — the EU's official medical-device database — is finally complete, actually doing it has become possible.
MD Atlas is the tool that turns it into a few seconds' work.
Record
The dispensing of implantable devices — UDI, patient ID, date.
Verify
The CE marking and certificate before you supply.
Follow
Recalls and status changes in the register.
How it works
A device's DataMatrix → its risk class, manufacturer, certificate and user manual, instantly. Or search the official EU register by name. Free, no commitment.
Follow the devices you supply. MD Atlas keeps an eye on their status in the EU register — withdrawn, recalled, certificate or UDI changes — and alerts you.
Every device already carries a DataMatrix: your customers scan it themselves in the MD Atlas app and open the manual. They never lose it again.
What it changes for you
If a device you supply changes status in the EU register — withdrawn, recalled — you're alerted, without having to check yourself. No more manual monitoring.
The due diligence the law asks of you, done in seconds: CE marking, certificate validity, notified body.
Device data and identifiers change over time, often silently. MD Atlas watches them for you.
The user manual, in your customers' pocket
Every device already carries a DataMatrix. Your customers scan it with the MD Atlas app and instantly open the official user manual — on their phone, any time. Nothing to keep, nothing to lose.
Invite your customers to use the app in-store: a simple service that sets your pharmacy apart.
Official user manual
Central venous catheter
[ Mockup — manual viewer ]
A real need, an official source
~20,000
pharmacies concerned in France
EUDAMED
the European Union's official register
15 yrs
retention of dispensing records
The information in MD Atlas comes straight from the European Union's official medical-device database (EUDAMED) — the very source your regulation points to. Official data, in your language as a pharmacist.
Pricing
Create your account — no card.
€0
Frequently asked questions
The data is public, but it isn't usable at the counter: EUDAMED asks for identifiers you don't have and answers in regulatory language. MD Atlas reads it for you, from a DataMatrix scan, in a pharmacist's words. Search, scanning and manuals stay free, with no subscription; the extras are metered in credits — automatic monitoring (be alerted to a status change without checking) and certificate-document downloads.
Yes. Under MDR Article 14, a pharmacy that supplies a CE-marked device is a distributor, with duties to verify CE marking, certificate and UDI and to act on recalls — in every EU country.
Not today — MD Atlas is a standalone tool that complements your system. Integration is on our roadmap. Use it now, change nothing.
Yes — it comes from EUDAMED, the European Union's official medical-device database.
Get started
Create your free account, scan your first device, and share a manual with a customer — in two minutes.