Low prices! Originals & Translations! Save your budget and time!
ONLINENORMS: Online Standards Store
Click View Shopping Cart
  1. Home
  2. DIN
  3. DIN EN 13532 PDF

DIN EN 13532 PDF

DIN EN 13532 PDF

Name:
DIN EN 13532 PDF

Published Date:
08/01/2002

Status:
Active

Description:

General requirements for in vitro diagnostic medical devices for self-testing; German version EN 13532:2002, German and English texts

Publisher:
DIN-adopted European Standard

Document status:
Active
Format:
Electronic (PDF)
Delivery time:
10 minutes
Delivery time (for Russian version):
200 business days
SKU:
Choose Document Language:
$20.274
Need Help?

File Size : 1 file , 230 KB
Note : This product is unavailable in Russia, Ukraine, Belarus
Number of Pages : 11
Product Code(s) : 9220714, 9220714
Published : 08/01/2002

History

Related products

DIN EN 12006-2
DIN EN 12006-2
Published Date: 08/01/2009
Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 2: Vascular prostheses including cardiac valve conduits (includes Amendment A1:2009)
$27.795
DIN EN 13640
DIN EN 13640
Published Date: 06/01/2002
Stability testing of in vitro diagnostic reagent; German version EN 13640:2002, German and English texts
$22.236
DIN EN 1422
DIN EN 1422
Published Date: 08/01/2014
Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
$48.723

Best-Selling Products

FDA 21 CFR PART 1020
FDA 21 CFR PART 1020
Published Date: 04/01/2020
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
$12.9
FDA 21 CFR PART 1020
FDA 21 CFR PART 1020
Published Date: 04/01/2019
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
$12.9
FDA 21 CFR PART 1020
FDA 21 CFR PART 1020
Published Date: 04/01/2016
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
$12.9
FDA 21 CFR PART 1020
FDA 21 CFR PART 1020
Published Date: 04/01/2021
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
$12.9
FDA 21 CFR PART 1040
FDA 21 CFR PART 1040
Published Date: 04/01/2021
PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS
$11.4
FDA 21 CFR PART 111
FDA 21 CFR PART 111
Published Date: 04/01/2020
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
$12.6