Linde France

Certificate DZ 2360710-1

Rev. 0Issued

Valid until: Dec 22, 2029

Certificate DZ 2360710-1 is a valid Quality assurance issued to Linde France and registered in EUDAMED. Valid until December 22, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number: DZ 2360710-1
Certificate type: Quality assurance
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 0197DZ 2360710-10

Validity

Issued: Dec 23, 2024
Valid from: Dec 23, 2024
Valid until: Dec 22, 2029

Manufacturer

Manufacturer: Linde France
Manufacturer SRN: FR-MF-000000961
Manufacturer country: France

Notified body

Notified body
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

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa4

4 scopes

V0901 – CLINICAL/THERAPEUTIC APPLICATIONS CARBON DIOXIDE
Class IIa
V0902 – CLINICAL/THERAPEUTIC APPLICATIONS LIQUID NITROGEN
Class IIa
V0904 – CLINICAL/THERAPEUTIC APPLICATIONS NITROUS OXIDE
Class IIa
K020499 - DEVICES FOR SURGERY WITH ARGON GAS GENERATOR, SINGLE-USE – OTHER
Class IIa

Documents

LanguagesEN