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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

3352 — Class I MDR by Alto Products Im- und…

MD Atlas
Alto Products Im- und Export GmbH

EUDAMED last updated this device on May 20, 2026

3352

4062684Ablaufbeutel-USB9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Alto Products Im- und Export GmbH
UDI-DI code: 04062684201094
Reference / catalog number: 3352

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Manufacturer information

Organization name: Alto Products Im- und Export GmbH
SRN: DE-MF-000010868
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	May 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04062684201094
Basic UDI-DI: 4062684Ablaufbeutel-USB9
Reference / catalog number: 3352
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: 500
Additional product description: Der Ablaufbeutel für Flüssigkeiten in der OP ist ein flexibler Sammelbeutel zur kontrollierten Aufnahme und Sammlung von während operativer Eingriffe anfallenden Flüssigkeiten.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 26 MU10
25 MU10

EMDN nomenclature code(s)

A06030499INTRA-OPERATION FLUID COLLECTION DEVICES - OTHER

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

07924062684Schutzkittel-US-7QOn 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.