Pure Global
7 Devices

JOTEC GmbH - Applicant Profile

Artivion (Formerly Cryolife)

JOTEC GmbH is associated with 7 medical devices registered under the Hong Kong Medical Device Administrative Control System (MDACS). Explore bilingual product names, risk classes, authorised representatives, and life-cycle milestones.

2 Risk Classes
Since 2016
Latest 2024
Applicant Overview
Bilingual manufacturer details sourced from Hong Kong MDACS.
Applicant (EN)
JOTEC GmbH
Country
Germany
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Applicant (ZH)
Artivion (Formerly Cryolife)
Address
Lotzenacker 23, 72379 Hechingen, Germany
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Recent MDACS Registrations
Latest 15 devices linked to this applicant.
DeviceRisk ClassAuthorised RepRegistered
Guide Wires
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II
Pacific Medical (Hong Kong) Company Limited
Aug 08, 2024
Catheters, Vascular, Angioplasty, Balloon
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II
Pacific Medical (Hong Kong) Company Limited
Jul 08, 2024
Stent/Grafts, Vascular, Aortic
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IV
Pacific Medical (Hong Kong) Company Limited
Feb 08, 2023
Stent/Grafts, Vascular, Peripheral
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IV
Pacific Medical (Hong Kong) Company Limited
Nov 23, 2022
Stent/Grafts, Vascular, Aortic
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IV
Pacific Medical (Hong Kong) Company Limited
Mar 14, 2022
Prostheses, Blood Vessel, Artificial
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IV
Pacific Medical (Hong Kong) Company Limited
Sep 03, 2021
Stent/Grafts, Vascular, Aortic
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IV
Prism JTC Limited
Jun 21, 2016
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Risk Class Breakdown
II2
IV5
Timeline
First Registration
Jun 21, 2016
Most Recent
Aug 08, 2024