Filme Opht-R

Organization name

Panin Srl

SRN

IT-MF-000020738

Manufacturer status

Active

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

• CW135

  EUDAMED did not publish a description for this code.
• CW277

  Although FILME OPHT-R is extremely tolerable, in some rare cases it may cause a stinging effect, irritation, ocular allergy or reddening. If this occurs, discontinue use and consult a doctor.
• CW999

  Individuals already assessed hypersensitivity to this product. Not to be injected, no to be swallowed. If you experience blurred vision after use refrain from driving or the use of machinery

Primary placement in Italy; available across 3 countries total.

Trade name

Filme Opht-R

UDI-DI code

08033837335047

Basic UDI-DI

B-08033837335047

Reference / catalog number

FEOPHTR

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

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.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• Q02030206EYE LUBRICANT SOLUTIONS

Certificate health across this manufacturer's portfolio.