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API STD 521: Guide for Pressure-relieving and Depressuring Systems – Edition 6

$

682

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API STD 653: Tank Inspection, Repair, Alteration, and Reconstruction – Edition 4

$

507

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CSA Z662:19 – Oil and gas pipeline systems

$

1197

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CSA Z341 Series-18: Storage of hydrocarbons in underground formations

$

878

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CSA Z246.2-14 – Emergency preparedness and response for petroleum and natural gas industry systems

$

596

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CSA Z341 Series:22 – Storage of hydrocarbons in underground formations

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878

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CSA Z731-09 (R2014) – Emergency Preparedness and Response

$

177

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CSA Z662:23 – Oil and gas pipeline systems

$

1197

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CSA Z341 Series:26 – Storage of Hydrocarbons in underground formations

$

878

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CSA B51:24 Boiler, Pressure Vessel, and Pressure Piping Code

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389

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ISO 12417:2022

ISO 12417:2022 Cardiovascular implants and extracorporeal systems – Vascular device-drug combination products – Part 2: Local regulatory information

CDN $295.00

SKU: 9757726a2a89 Category:

Description

This document provides region-specific information for:

-    local submissions and approvals for vascular device-drug combination products (VDDCPs) in countries and regions around the world;

-    changes related to the drug-containing part and how they are evaluated by different local regions.

For implanted products, this document is considered as a supplement to ISO 14630, which specifies general requirements for the performance of non-active surgical implants.

This document is considered also as a supplement to ISO 12417-1, and any relevant device-specific standards, such as the ISO 25539 series specifying requirements for endovascular devices. This document also addresses VDDCPs that are not necessarily permanent implants.

Edition

2

Published Date

2022-07-07

Status

PUBLISHED

Pages

29

Language Detail Icon

English

Format Secure Icon

Secure PDF

Abstract

This document provides region-specific information for:

-    local submissions and approvals for vascular device-drug combination products (VDDCPs) in countries and regions around the world;

-    changes related to the drug-containing part and how they are evaluated by different local regions.

For implanted products, this document is considered as a supplement to ISO 14630, which specifies general requirements for the performance of non-active surgical implants.

This document is considered also as a supplement to ISO 12417-1, and any relevant device-specific standards, such as the ISO 25539 series specifying requirements for endovascular devices. This document also addresses VDDCPs that are not necessarily permanent implants.

Previous Editions

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