BS EN IEC 61300-2-11:2024 PDF

Name:
BS EN IEC 61300-2-11:2024 PDF

Published Date:
01/25/2024

Status:
Active

Description:

Fibre optic interconnecting devices and passive components. Basic test and measurement procedures-Tests. Axial compression

Publisher:
British-Adopted European Standard

Document status:

Active

Format:

Electronic (PDF)

Delivery time:

10 minutes

Delivery time (for Russian version):

200 business days

SKU:

All current amendments available at time of purchase are included with the purchase of this document.

File Size :	1 file , 770 KB
ISBN(s) :	9780539191677
Note :	This product is unavailable in Ukraine, Russia, Belarus
Number of Pages :	14
Product Code(s) :	30443251, 30443251, 30443251
Published :	01/25/2024

History

BS EN IEC 61300-2-11:2024

Published Date: 01/25/2024

Fibre optic interconnecting devices and passive components. Basic test and measurement procedures-Tests. Axial compression

$48.006

BS EN 61300-2-11:1997

Published Date: 10/15/1997

Fibre optic interconnecting devices and passive components. Basic test and measurement procedures. Tests-Axial compression

$48.006

Related products

BS EN 62148-2:2011

Published Date: 02/28/2011

Fibre optic active components and devices. Package and interface standards-SFF 10-pin transceivers

$57.15

BS EN 61753-062-6:2008

Published Date: 02/29/2008

Fibre optic interconnecting devices and passive components performance standard-Non-connectorized single-mode fibre optic pigtailed isolators for category O. Uncontrolled environment and sequential test

$57.15

Best-Selling Products

MEDDEV 13/93

Published Date:

Guidelines Relating to the Application of: The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices

MEDDEV 2.1/3

Published Date: 03/01/1998

Guidelines Relating to the Demarcation Between 90/385/EEC on Active Implatable Medical Devices, 93/42/EEC on Medical Devices,65/65/EEC Relating to Medicinal Products & Related Directives

MEDDEV 3/94

Published Date: 04/01/1994

Guidelines Relating to the Application of : The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices