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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

E1605 — Class I MDD by S.C. EMINVEST…

MD Atlas
S.C. EMINVEST PHARMACEUTICALS S.R.L.

EUDAMED last updated this device on Jul 10, 2025

E1605

B-EuRhoVital4S

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: S.C. EMINVEST PHARMACEUTICALS S.R.L.
UDI-DI code: D-EuRhoVital4S
Reference / catalog number: E1605

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Manufacturer information

Organization name: S.C. EMINVEST PHARMACEUTICALS S.R.L.
SRN: RO-MF-000001412
Manufacturer status: Active

Critical warnings

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

CW010
For more information read the leaflet carefully
CW007
Do not use if the packaging is damaged or shows signs of use
CW032
Do not use the product after the expiry date specified on the packaging
CW135
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jul 31, 2025	Dec 31, 2028

Device identification

Trade name: not provided
UDI-DI code: D-EuRhoVital4S
Basic UDI-DI: B-EuRhoVital4S
Reference / catalog number: E1605
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

D-EuRhoVital4S

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

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

Q030103NASAL IRRIGATION SOLUTIONS

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

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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.