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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

F1340CCCK — Class I MDR by DIFFUPLAST srl

MD Atlas
DIFFUPLAST srl

EUDAMED last updated this device on May 18, 2026

F1340CCCK

805815978SPYV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DIFFUPLAST srl
UDI-DI code: 28058159784322
Reference / catalog number: F1340CCCK

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View device family (Basic UDI)

Manufacturer information

Organization name: DIFFUPLAST srl
SRN: IT-MF-000022506
Manufacturer status: Active

Related devices

E1420OD805815978SPYVOn the market E1405OD805815978SPYVOn the market E1402OD5805815978SPYVOn the market E1401OD805815978SPYVOn the market E1401OD5805815978SPYVOn 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

4 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.
CW011
Refer to technical specification for material composition before use Do not use needle more than 23 gauge

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 28058159784322
Basic UDI-DI: 805815978SPYV
Reference / catalog number: F1340CCCK
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: 5
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 4000 MU03

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)28058159784322

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

A080102PARENTERAL FEEDING BAGS AND CONTAINERS (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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