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

HYALOSAN Lubricant gel with… — Class IIb MDR

MD Atlas
Dr. Müller Pharma s.r.o.

EUDAMED last updated this device on Mar 11, 2026

HYALOSAN Lubricant gel with hyaluronic acid

85956104LGHAW6

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dr. Müller Pharma s.r.o.
UDI-DI code: 08595610403539
Reference / catalog number: PC0270_002

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: Dr. Müller Pharma s.r.o.
SRN: CZ-MF-000000005
Manufacturer status: Active

Related devices

PC0203_01485956104LGGSOn the market PC8903_00285956104PSHWOn the market PC8901_00385956104PSHWOn the market ANGINAL® Oral Spray with Tea Tree Oil85956104PSHWOn the market PC8903_00185956104PSHWOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Czechia; available across 2 countries total.

Country	On market since	Until
CzechiaPrimary placement	Mar 25, 2019	Still on market
Slovakia	Mar 25, 2019	Still on market

Device identification

Trade name: HYALOSAN Lubricant gel with hyaluronic acid
UDI-DI code: 08595610403539
Basic UDI-DI: 85956104LGHAW6
Reference / catalog number: PC0270_002
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M9002PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

2023-MDR/QS-035/BSupplemented
Quality management systemNotified body: 2265Expiry: Oct 20, 2028
2023-MDR/QS-034/CSupplemented
Quality management systemNotified body: 2265Expiry: Oct 20, 2028
2023-MDR/QS-033/BSupplemented
Quality management systemNotified body: 2265Expiry: Oct 20, 2028
2023-MDR/QS-031refdata.certificate-status.reissued
Quality management systemNotified body: 2265Expiry: Oct 20, 2028
2023-MDR/QS-032Issued
Quality management systemNotified body: 2265Expiry: Oct 20, 2028

2023-MDR/QS-031

Issued

Quality management systemNotified body: 2265Expiry: Oct 20, 2028