Chetan Meditech Pvt. Ltd.

Certificate 2024-MDR/TD-031

Rev. 00Issued

Valid until: Jul 1, 2029

Certificate 2024-MDR/TD-031 is a valid Technical documentation issued to Chetan Meditech Pvt. Ltd. and registered in EUDAMED. Valid until July 1, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number: 2024-MDR/TD-031
Certificate type: Technical documentation
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 22652024-MDR/TD-03100

Validity

Issued: Jul 1, 2024
Valid from: Jul 1, 2024
Valid until: Jul 1, 2029

Manufacturer

Manufacturer
Manufacturer SRN: IN-MF-000013541
Manufacturer country: India

Notified body

Notified body
Notified body SRN: 2265
Notified body country: Slovakia

Covered devices

BIOTEK, BIO-VIM, BIO-VIM LRP, BIO-VIM LRT, ARTHROVIMS BR AnchorClass III
89042103cmplimp001X7

Linked SSCPs

SSCP SSCP/01

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

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified1

1 scope

BIOTEK, BIO-VIM, BIO-VIM LRP, BIO-VIM LRT, ARTHROVIMS BR Anchor
89042103cmplimp001X7

Documents

LanguagesEN