EUDAMED last updated this device on May 21, 2026

Disposable infusion pump

B-06952803711482

On the marketClass IIb

Applicable legislation: —
Organization name: Zhejiang Fert Medical Device Co.,Ltd.
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 06952803711482
Reference / catalog number: E100002001

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

Disposable infusion pump is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Zhejiang Fert Medical Device Co.,Ltd.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: Disposable infusion pump
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 06952803711482
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: B-06952803711482
Reference / catalog number: E100002001
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Classification

Risk category: Class IIb
Applicable legislation: —
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

Encoded

(01)06952803711482

EMDN nomenclature code(s)

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

A05010201ELASTOMERIC SYSTEMS - VARIABLE FLOW W/O ADDITIONAL BOLUS

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

Caution
For single patient and single-use only. Not to be re-sterilized or reused, in which case performance of device can be affected, and risk of cross-infection is increased.

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Feb 17, 2024	Dec 31, 2028

Disposable infusion pump

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Market distribution

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Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Certificates covering this device

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Manufacturer information

Certificates covering this device

Certificates

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