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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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MD Atlas
Documents

Aesculap AG

Certificate 20333GB450240524

Issued

Valid until: May 23, 2029

Overview

Certificate number: 20333GB450240524
Certificate type: Technical documentation
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 048220333GB450240524

Validity

Issued: May 24, 2024
Valid from: May 24, 2024
Valid until: May 23, 2029

Manufacturer

Manufacturer: Aesculap AG
Manufacturer SRN: DE-MF-000005504
Manufacturer country: Germany

Notified body

Notified body: DNV MEDCERT GmbH
Notified body SRN: 0482
Notified body country: Germany

Covered devices

ENNOVATE C lamina hookClass III
40392390000022922N

Characteristics

Sterile: —
Human tissues: —
Animal tissues: —
In vitro diagnostics: —
Initial registration: Yes
New device: No
Discard allowed: No
SSCP enabled: Yes
Mechanism of scrutiny: No
Intended medical purpose: —
SPP applicable: —
Conditions applicable: No
MOS outside EUDAMED: —
QMS/MOS type: Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified1

1 scope

ENNOVATE C lamina hook
40392390000022922N

Documents

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