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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

Kit con 6 siringhe enterali 20 ml… — Class IIa MDR

MD Atlas
PENTAFERTE ITALIA SRL

EUDAMED last updated this device on Dec 22, 2025

Kit con 6 siringhe enterali 20 ml enfit + 1 cannula 20 ml enfit + 1 cannula 20 GD enfit + 8 tappi maschio enfit + 6 prolunghe enfit: in vassoio sterile monouso - NUTRIFIT

80152621054W

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PENTAFERTE ITALIA SRL
UDI-DI code: 08015262022167
Reference / catalog number: 1025.726

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View device family (Basic UDI)

Manufacturer information

Organization name: PENTAFERTE ITALIA SRL
SRN: IT-MF-000040982
Manufacturer status: Active

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Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW999
Single sterile barriersystem with protective packaging inside

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Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: Kit con 6 siringhe enterali 20 ml enfit + 1 cannula 20 ml enfit + 1 cannula 20 GD enfit + 8 tappi maschio enfit + 6 prolunghe enfit: in vassoio sterile monouso - NUTRIFIT
UDI-DI code: 08015262022167
Basic UDI-DI: 80152621054W
Reference / catalog number: 1025.726
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 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

EMDN nomenclature code(s)

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

A030403ENTERAL NUTRITION KITS (INCLUDING THOSE VIA PUMP), SINGLE-USE

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.