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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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Organization name
UDI-DI code
Reference / catalog number

55.0647 — Class IIb MDR by URSAPHARM Arzneimittel…

MD Atlas
URSAPHARM Arzneimittel GmbH

EUDAMED last updated this device on Mar 13, 2026

55.0647

4031626101888PR

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: URSAPHARM Arzneimittel GmbH
UDI-DI code: 04031626001801
Reference / catalog number: 55.0647

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Manufacturer information

Organization name: URSAPHARM Arzneimittel GmbH
SRN: DE-MF-000007748
Manufacturer status: Active

Related devices

55.14114031626101365NLOn the market 55.03964031626101365NLOn the market EvoTears4031626551134RAOn the market 56.00654031626551134RAOn the market EvoTears4031626551134RAOn 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.

Critical warnings

7 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW135
EUDAMED did not publish a description for this code.
CW262
EUDAMED did not publish a description for this code.
CW999
Las pomadas oftálmicas deben usarse evitando el contacto de la punta del tubo con el ojo o la piel.
CW999
En caso de utilizar VitA POS durante el día, su visión se verá afectada durante algún tiempo debido a la consistencia grasa de la pomada. Hasta que desaparezca, no debe conducir, utilizar máquinas ni trabajar sin una base estable.
CW999
CONTRAINDICACIONES VitA POS no debería aplicarse - en casos de hipersensibilidad a alguno de sus componentes. - con lentes de contacto. - después de intervenciones quirúrgicas oftálmicas ni en caso de lesiones agudas en el ojo, ya que no hay estudios clínicos al respecto.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Feb 1, 2009	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04031626001801
Basic UDI-DI: 4031626101888PR
Reference / catalog number: 55.0647
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: VitA POS es una pomada estéril con vitamina A para uso ocular.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q02030399OPHTHALMOLOGY, VISCOELASTIC FLUIDS - OTHER

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