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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

aluetta 20mg — Class I MDR by Ares Trading SA

MD Atlas
Ares Trading SA

EUDAMED last updated this device on Sep 21, 2022

aluetta 20mg

4054839aluettaHJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ares Trading SA
UDI-DI code: 04065266537000
Reference / catalog number: U122221D

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Manufacturer information

Organization name: Ares Trading SA
SRN: CH-MF-000021799
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market

Device identification

Trade name: aluetta 20mg
UDI-DI code: 04065266537000
Basic UDI-DI: 4054839aluettaHJ
Reference / catalog number: U122221D
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: ALUETTA PEN 20MG (1)-MS-WEU5
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - 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

aluetta 12mg4054839aluettaHJOn the market aluetta 12mg4054839aluettaHJOn the market aluetta 12mg4054839aluettaHJOn the market aluetta 12mg4054839aluettaHJOn the market U122220Z4054839aluettaHJOn 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.