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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

PRODF041010 — Class I MDR by PRODCONFARM SRL

MD Atlas
PRODCONFARM SRL

EUDAMED last updated this device on Apr 12, 2024

PRODF041010

5944759041PRODF0410106D

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PRODCONFARM SRL
UDI-DI code: 05944759041417
Reference / catalog number: PRODF041010

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Manufacturer information

Organization name: PRODCONFARM SRL
SRN: RO-MF-000017975
Manufacturer status: Active

Critical warnings

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

CW009
De unica folosinta
CW007
Verificati integritatea ambalajului inainte de utilizare A nu se utiliza daca ambalajul este deteriorat
CW032
Verificati data expirarii produsului inainte de utilizare

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Market distribution

Primary placement in Romania; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05944759041417
Basic UDI-DI: 5944759041PRODF0410106D
Reference / catalog number: PRODF041010
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: FESI TIFON 10/10 40 gr ± 2
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

EMDN nomenclature code(s)

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

M030101HYDROPHILIC GAUZE BANDAGES

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.