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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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Bausch & Lomb GmbH

Certificate HZ 1333770-1

Rev. 0Issued
Valid until
Apr 26, 2028

Certificate HZ 1333770-1 is a valid Quality management system issued to Bausch & Lomb GmbH and registered in EUDAMED. Valid until April 26, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
HZ 1333770-1
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0197HZ 1333770-10

Validity

Issued
Apr 27, 2023
Valid from
Apr 27, 2023
Valid until
Apr 26, 2028

Notified body

Notified body
TÜV Rheinland LGA Products GmbH
Notified body SRN
0197
Notified body country
Germany

Covered devices

No specific devices are listed for this certificate.

Characteristics

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

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa1

1 scope

  • Q021101 - Occular irrigation and aspiration cannulas, single use
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
Bausch & Lomb GmbH
Manufacturer SRN
DE-MF-000009142
Manufacturer country
Germany