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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

20015429 — Class IIa MDD by milon industries GmbH

MD Atlas
milon industries GmbH

EUDAMED last updated this device on Sep 8, 2023

20015429

B-04262401914294

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: milon industries GmbH
UDI-DI code: 04262401914294
Reference / catalog number: 20015429

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Manufacturer information

Organization name: milon industries GmbH
SRN: DE-MF-000009930
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Sep 1, 2018	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262401914294
Basic UDI-DI: B-04262401914294
Reference / catalog number: 20015429
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Stationary training equipment
Additional information URL: https://milongroup.com/de/milon-q/lat-pulldown
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0899MEDICAL SUPPORT EQUIPMENT - 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

20016243B-04262401912436On the market 20015431B-04262401914317On the market 20015398B-04262401913983On the market 20015405B-04262401914058On the market 20015400B-04262401914003On 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.