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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

PRODF041020 — Class I MDR by PRODCONFARM SRL

MD Atlas
PRODCONFARM SRL

EUDAMED last updated this device on Apr 12, 2024

PRODF041020

5944759041PRODF0410206G

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PRODCONFARM SRL
UDI-DI code: 05944759041431
Reference / catalog number: PRODF041020

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View device family (Basic UDI)

Manufacturer information

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

Related devices

PRODT045944759041PRODT045ZOn the market PRODT035944759041PRODT035XOn the market PRODF0110105944759041PRODF0110105COn the market PRODT015944759041PRODT015TOn the market PRODF0310105944759041PRODF03101062On 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

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: 05944759041431
Basic UDI-DI: 5944759041PRODF0410206G
Reference / catalog number: PRODF041020
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 10/20 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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