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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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CITOTEST LABWARE MANUFACTURING CO.,LTD

Certificate DZ 2029176-1

Rev. 0Issued
Valid until
May 29, 2028

Certificate DZ 2029176-1 is a valid Quality assurance issued to CITOTEST LABWARE MANUFACTURING CO.,LTD and registered in EUDAMED. Valid until May 29, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
DZ 2029176-1
Certificate type
Quality assurance
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0197DZ 2029176-10

Validity

Issued
May 30, 2023
Valid from
May 30, 2023
Valid until
May 29, 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
Yes
Human tissues
No
Animal tissues
No
In vitro diagnostics
No
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
No
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 I1

1 scope

  • A1101 SAMPLE COLLECTION NEUTRAL SWABS - Classical swabs - Transport swabs U089002-DEVICES FOR GYNAECOLOGICAL CYTOLOGY - Cytology brushes
    Class I

Documents

LanguagesEN

Manufacturer

Manufacturer
CITOTEST LABWARE MANUFACTURING CO.,LTD
Manufacturer SRN
CN-MF-000017214
Manufacturer country
China