Medicontur Medical Engineering Ltd.

Certificate 2023-MDR/TD-048/A

Rev. 01Supplemented

Valid until: Nov 10, 2028

Certificate 2023-MDR/TD-048/A is a valid Technical documentation issued to Medicontur Medical Engineering Ltd. and registered in EUDAMED. Valid until November 10, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number: 2023-MDR/TD-048/A
Certificate type: Technical documentation
Certificate status: Supplemented
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 22652023-MDR/TD-048/A01

Validity

Issued: Dec 12, 2024
Valid from: Dec 12, 2024
Valid until: Nov 10, 2028

Notified body

Notified body: 3EC International a.s.
Notified body SRN: 2265
Notified body country: Slovakia

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

Status changes

Supplemented

Supersedes

2023-MDR/TD-048IssuedNov 10, 2023 → Nov 10, 2028

Predecessor certificate not registered in EUDAMED.

Scope coverage

Unspecified34

34 scopes

Device
599302613ADWQ
Device
599302640PMYV
Device
599302640PD5
Device
599302677ADYN
Device
599302677PE9
Device
599302677TA2C
Device
599302677ME3
Device
599302677MT2V
Device
599302677CTARP
Device
599302640ADWW
Device
599302690TAZL
Device
599302690CMYR
Device
599302690CTAQU
Device
599302690ADXZ
Device
599302677ADYRD
Device
599302640ADYNT
Device
599302677PY3G
Device
599302677TAYU3
Device
599302677MY37
Device
599302677MTYUR

1 / 2

Documents

LanguagesEN