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Medical Device Division · registration 220390Active

JOTEC

Hong KongStent/Grafts, Vascular, PeripheralClass IVJOTEC GmbH
Official record identity
MDACS listing number
220390
Model name
E-ventus BX Peripheral Stent Graft System (91BX1805L-00, 91BX2205L-00, 91BX2805L-00, 91BX3805L-00, 91BX5805L-00, 91BX1806L-00, 91BX2206L-00, 91BX2806L-00, 91BX3806L-00, 91BX5806L-00, 91BX1807L-00, 91BX2307L-00, 91BX2707L-00, 91BX3707L-00, 91BX5707L-00, 91BX1808L-00, 91BX2708L-00, 91BX3708L-00, 91BX5708L-00, 91BX1809L-00, 91BX2709L-00, 91BX3709L-00, 91BX5709L-00, 91BX1810L-00, 91BX2710L-00, 91BX3710L-00, 91BX5710L-00)
Registration date
November 23, 2022
Expiry date
November 23, 2027
Source update date
July 09, 2025
Status
Active
Official value: Valid
Classification
Risk class
Class IV
Official value: IV
Published category
Stent/Grafts, Vascular, Peripheral
Published parties
Registrant / registration holder
Pacific Medical (Hong Kong) Company Limited
Manufacturer
JOTEC GmbH
Official description

Stent/Grafts, Vascular, Peripheral

Additional source fields
AMD nomenclature code
20455
Local responsible person phone
23438009
Published manufacturer address
Lotzenaecker 23, 72379 Hechingen, Germany
About this record

This page mirrors one official MDACS listing. Roman-numeral classes use Hong Kong’s general medical-device scheme, while letter classes use the IVD scheme. Valid, expired, and delisted records remain distinguishable; no mixed classification scale is fabricated.