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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

Self-retaining retractor — Class I MDD by Atesos medical AG

MD Atlas
Atesos medical AG

EUDAMED last updated this device on Jan 11, 2022

Self-retaining retractor

B-07640164282589

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Atesos medical AG
UDI-DI code: 07640164282589
Reference / catalog number: 800240

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Manufacturer information

Organization name: Atesos medical AG
SRN: CH-MF-000010304
Manufacturer status: Active

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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.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Apr 25, 2024
Italy		Apr 25, 2024

Device identification

Trade name: Self-retaining retractor
UDI-DI code: 07640164282589
Basic UDI-DI: B-07640164282589
Reference / catalog number: 800240
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Wundspreizer für anterioren MIS Zugang Hüft TEP
Additional information URL: https://atesos.ch/wp-content/uploads/2021/11/509.D002-A1-Bedienungsanleitung_DAASS-Wundspreizrahmen.pdf
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L0915SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, REUSABLE

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

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Expiration date
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Software identification