REGISTER

FR
Search
×
FR

Placeholder headline

This is just a placeholder headline

API TR 2583 : Measurement of Produced Water for Custody Transfer

$

174

BUY NOW

Placeholder headline

This is just a placeholder headline

API TR 2581: Wet Gas Sampling

$

189

BUY NOW

Placeholder headline

This is just a placeholder headline

API TR 2581 Wet Gas Sampling : Errata 1

$

0

BUY NOW

Placeholder headline

This is just a placeholder headline

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

$

481

BUY NOW

Placeholder headline

This is just a placeholder headline

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

$

208

BUY NOW

Placeholder headline

This is just a placeholder headline

API 510: Errata 2

$

0

BUY NOW

Placeholder headline

This is just a placeholder headline

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

$

189

BUY NOW

Placeholder headline

This is just a placeholder headline

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

$

518

BUY NOW

Placeholder headline

This is just a placeholder headline

API SPEC 5CT: Casing and Tubing Addendum 1

$

0

BUY NOW

Placeholder headline

This is just a placeholder headline

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

$

301

BUY NOW

ISO 20698:2018

ISO 20698:2018 Catheter systems for neuraxial application – Sterile and single-use catheters and accessories

CDN $233.00

SKU: 5b934a891aa5 Categories: ,

Description

This document specifies general requirements and test methods for catheter systems intended to be used in neuraxial applications.

This document specifies requirements for intended performance, design attributes, materials, design evaluation, manufacture, sterilization, packaging and information supplied by the manufacturer, and tests to demonstrate conformity with these requirements.

Catheters for neuraxial applications are intended to administer medications directly into neuraxial sites, to deliver wound infiltration analgesia and to other regional analgesia procedures or to monitor or remove fluids from neuraxial sites for therapeutic or diagnostic purposes.

NOTE 1 Sites for the neuraxial application include the spine, intrathecal or subarachnoid space and the epi-, extra-, or peri-dural space (applications mentioned are just examples and not an exhaustive list). In neuraxial application, anaesthetics/analgesics can be administered regionally affecting a large part of the body, such as a limb, and include plexus blocks, such as the brachial plexus blocks or single nerve blocks. Neuraxial application procedures include continuous infusion of wounds with local anaesthetic agents.

NOTE 2 Local anaesthesia/analgesia injected hypodermically and systemic injection of anaesthetics are not considered neuraxial applications.

This document is applicable to the following types of devices:

– spinal/epidural catheter systems;

– spinal/epidural port catheter systems;

– peripheral nerve block catheter systems;

– wound infusion catheter systems (also known as catheters for Surgical Site Continuous Analgesia).

This document is not applicable to:

– pumps and other devices intended to deliver medications through these catheter systems;

– catheters generically intended to administer substances into the body which are not intended to interact directly with the nervous system, but which have an indirect effect on nervous system (e.g. cannula needles);

– drainage catheters for any other application than neuraxial.

Edition

1

Published Date

2018-07-26

Status

PUBLISHED

Pages

20

Language Detail Icon

English

Format Secure Icon

Secure PDF

Abstract

This document specifies general requirements and test methods for catheter systems intended to be used in neuraxial applications.

This document specifies requirements for intended performance, design attributes, materials, design evaluation, manufacture, sterilization, packaging and information supplied by the manufacturer, and tests to demonstrate conformity with these requirements.

Catheters for neuraxial applications are intended to administer medications directly into neuraxial sites, to deliver wound infiltration analgesia and to other regional analgesia procedures or to monitor or remove fluids from neuraxial sites for therapeutic or diagnostic purposes.

NOTE 1 Sites for the neuraxial application include the spine, intrathecal or subarachnoid space and the epi-, extra-, or peri-dural space (applications mentioned are just examples and not an exhaustive list). In neuraxial application, anaesthetics/analgesics can be administered regionally affecting a large part of the body, such as a limb, and include plexus blocks, such as the brachial plexus blocks or single nerve blocks. Neuraxial application procedures include continuous infusion of wounds with local anaesthetic agents.

NOTE 2 Local anaesthesia/analgesia injected hypodermically and systemic injection of anaesthetics are not considered neuraxial applications.

This document is applicable to the following types of devices:

- spinal/epidural catheter systems;

- spinal/epidural port catheter systems;

- peripheral nerve block catheter systems;

- wound infusion catheter systems (also known as catheters for Surgical Site Continuous Analgesia).

This document is not applicable to:

- pumps and other devices intended to deliver medications through these catheter systems;

- catheters generically intended to administer substances into the body which are not intended to interact directly with the nervous system, but which have an indirect effect on nervous system (e.g. cannula needles);

- drainage catheters for any other application than neuraxial.

Previous Editions

Can’t find what you are looking for?

Please contact us at: