Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

31010 — IVDR Class A IVDR by REAGENS Fejlesztő,…

MD Atlas
REAGENS Fejlesztő, Gyártó és Kereskedelmi Kft.

EUDAMED last updated this device on May 26, 2022

31010

599654731RQUICK4Z

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: REAGENS Fejlesztő, Gyártó és Kereskedelmi Kft.
UDI-DI code: 05996547310106
Reference / catalog number: 31010

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: REAGENS Fejlesztő, Gyártó és Kereskedelmi Kft.
SRN: HU-MF-000019161
Manufacturer status: Active

Related devices

ACTIVE PAPAIN Lyophilized599654721LIOPAPX2On the market 13110-01599654713AGGILN5On the market 131025996547130BROMEK3On the market 131015996547130BROMEK3On the market 131035996547130BROMEK3On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Hungary; available across 1 country total.

Placed on the market in Hungary; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05996547310106
Basic UDI-DI: 599654731RQUICK4Z
Reference / catalog number: 31010
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: REAG-QUICK Panoptic 3x1000 ml
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0103010399HAEMATOLOGY STAINS FOR MICROSCOPY - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification