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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

84353737SUEROFISN5 — Class I MDD by LABORATORIO REIG JOFRE,…

MD Atlas
LABORATORIO REIG JOFRE, S.A.

EUDAMED last updated this device on Jul 18, 2022

84353737SUEROFISN5

B-84353737SUEROFISN5XV

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: LABORATORIO REIG JOFRE, S.A.
UDI-DI code: D-84353737SUEROFISN5XV
Reference / catalog number: 84353737SUEROFISN5

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Manufacturer information

Organization name: LABORATORIO REIG JOFRE, S.A.
SRN: ES-MF-000010862
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: D-84353737SUEROFISN5XV
Basic UDI-DI: B-84353737SUEROFISN5XV
Reference / catalog number: 84353737SUEROFISN5
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: SUERO FISIOLÓGICO ORRAVAN GOTAS is a medical device intended by the manufacturer to be used as an aqueous solution of NaCl to be introduced into the nostril in order to eliminate excess mucus and allow good ventilation. The application of SUERO FISIOLÓGICO ORRAVAN GOTAS in the nostril humidifies the mucous membranes with the consequent decrease in the viscosity of the mucus. This allows its mobilization and elimination.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

D99DISINFECTANTS, ANTISEPTICS, STERILISING AGENTS AND DETERGENTS FOR MEDICAL DEVICES - 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

Related devices

84353737MILROSINA2RB-84353737MILROSINA2RJWOn the market 84353737OTOSPRAYRCB-84353737OTOSPRAYRC6ZOn the market 84353737SUENTILLASYYB-84353737SUENTILLASYY2FOn 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.