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API TR 2583 : Measurement of Produced Water for Custody Transfer

$

174

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API TR 2581: Wet Gas Sampling

$

189

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API TR 2581 Wet Gas Sampling : Errata 1

$

0

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API 510: Pressure Vessel Inspection Code: In-service Inspection, Rating, Repair, and Alteration

$

481

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API SPEC 6AV1: Validation of Safety and Shutdown Valves for Sandy Service : Edition 4

$

208

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API 510: Errata 2

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0

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API SPEC 16B Coiled Tubing, Snubbing and Wireline Well Intervention Equipment

$

189

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API SPEC 5CT: Casing and Tubing w/ Addendum 1

$

518

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API SPEC 5CT: Casing and Tubing Addendum 1

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0

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API RP 1161: Hazardous Liquid Pipeline Operator Qualification (OQ) : Edition 6

$

301

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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 $273.00

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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