AENOR UNE-EN ISO 8980-2 PDF

AENOR UNE-EN ISO 8980-2 PDF

Name:
AENOR UNE-EN ISO 8980-2 PDF

Published Date:
09/24/2004

Status:
[ Revised ]

Description:

Óptica oftálmica. Lentes terminadas sin biselar para gafas. Parte 2: Especificaciones para lentes progresivas. (ISO 8980-2:2004).

Publisher:
Spanish Association for Standardization and Certification

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Czech version):
200 business days

SKU:
aenor-une-en-iso-8980-2_2708449

Choose Document Language:
19.50 €
Need Help?
ENGLISH


Edition : 04
File Size : 2 files , 260 KB
Number of Pages : 18
Published : 09/24/2004

History


Related products

AENOR UNE 26045
Published Date: 06/01/1951
RACORES PARA EL EMPALME DE TUBOS. TIPOS CON OJIVA DE CIERRE. CONJUNTO
4.80 €
AENOR UNE-EN ISO 7441
Published Date: 07/08/2015
Corrosión de los metales y aleaciones. Determinación de la corrosión bimetálica mediante ensayos de exposición a corrosión atmosférica. (ISO 7441:2015).
22.20 €
AENOR UNE-EN ISO 1833-7
Published Date: 01/10/2018
Textiles - Quantitative chemical analysis - Part 7: Mixtures of polyamide with certain other fibres (method using formic acid) (ISO 1833-7:2017)
19.20 €
AENOR UNE-EN 60335-2-35
Published Date: 04/20/2016
Aparatos electrodomésticos y análogos. Seguridad. Parte 2-35: Requisitos particulares para calentadores de agua instantáneos.
24.00 €

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