companydirectorylist.com  Global Business Directories and Company Directories
Search Business,Company,Industry :


Country Lists
USA Company Directories
Canada Business Lists
Australia Business Directories
France Company Lists
Italy Company Lists
Spain Company Directories
Switzerland Business Lists
Austria Company Directories
Belgium Business Directories
Hong Kong Company Lists
China Business Lists
Taiwan Company Lists
United Arab Emirates Company Directories


Industry Catalogs
USA Industry Directories












Company Directories & Business Directories

MDR SALES; INC

WAXAHACHIE-USA

Company Name:
Corporate Name:
MDR SALES; INC
Company Title:  
Company Description:  
Keywords to Search:  
Company Address: 15391 E. Interstate 20,WAXAHACHIE,TX,USA 
ZIP Code:
Postal Code:
75168 
Telephone Number: 2147557172 (+1-214-755-7172) 
Fax Number:  
Website:
peckerpad. com 
Email:
 
USA SIC Code(Standard Industrial Classification Code):
5311 
USA SIC Description:
Retail shops 
Number of Employees:
 
Sales Amount:
 
Credit History:
Credit Report:
 
Contact Person:
 
Remove my name



copy and paste this google map to your website or blog!

Press copy button and paste into your blog or website.
(Please switch to 'HTML' mode when posting into your blog. Examples:
WordPress Example, Blogger Example)









Input Form:Deal with this potential dealer,buyer,seller,supplier,manufacturer,exporter,importer

(Any information to deal,buy, sell, quote for products or service)

Your Subject:
Your Comment or Review:
Security Code:



Previous company profile:
CNB COMMUNICATIONS
MCDOWELL CUSTOM HOMES; INC
FARM SALVAGE CONNECTION
Next company profile:
TURNER MIDDLE SCHOOL
CROWN DISTRIBUTING
FEARIS APPRAISALS










Company News:
  • 2017 745 - EN - Medical Device Regulation - EUR-Lex
    However, a fundamental revision of those Directives is needed to establish a robust, transparent, predictable and sustainable regulatory framework for medical devices which ensures a high level of safety and health whilst supporting innovation
  • Medical Device Reporting (MDR): How to Report Medical Device Problems
    Medical Device Reporting (MDR) is one of the postmarket surveillance tools the FDA uses to monitor device performance, detect potential device-related safety issues, and contribute to
  • EU Medical Device Regulation MDR: Everything you need to know
    Medical Device Regulation MDR (2017 745)… Manufacturers who wish to place medical devices on the market in the EU must comply with the European Medical Device Regulation MDR
  • MDR vs MXDR: What’s the Difference? - SentinelOne
    Managed Detection and Response (MDR) is a focused cybersecurity service It detects and responds to threats at the network and endpoint level Think of endpoints as touchpoints—like servers, computers, or any connected devices that are often prime targets for cyber threats
  • mdr. de – Radio, Fernsehen, Nachrichten für Mitteldeutschland
    Mehr als 600 Einsatzkräfte kämpfen weiter gegen den Waldbrand in der munitionsbelasteten Gohrischheide Unter ihnen ist auch der Gröditzer Feuerwehrmann Oliver Linge, den der Anblick seiner Heimat
  • Medical Device Regulation (MDR) - TÜV SÜD
    With more than 750 medical device professionals in more than 30 locations worldwide, we are one of the largest EU Notified Bodies globally authorised to provide certification services under the MDR
  • Guidance - MDCG endorsed documents and other guidance
    Regulation (EU) 2017 745 on medical devices (MDR) and Regulation (EU) 2017 746 (IVDR) on in vitro diagnostic medical devices The majority of documents on this page are endorsed by the Medical Device Coordination Group (MDCG) in accordance with Article 105 of the MDR and Article 99 of the IVDR
  • Download the dental manual instruction and guidance - Yucera
    Download the dental manual instruction and guidance | Yucera | page No 【1】 - In Yucera Download Center, You can download our machine operation manual, product parameters, as well as additional operation skill instruction manuals and more
  • 1-4 U. S. FOOD DRUG
    21 CFR Part 807 97) For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
  • A GUIDE TO THE NEW EUROPEAN UNION MEDICAL DEVICE REGULATION (MDR)
    Compliance with the MDR is mandatory for all companies that manufacture, import, and distribute medical devices in Europe, including companies that sell medical gloves and masks The European Council introduced the MDR for several reasons




Business Directories,Company Directories
Business Directories,Company Directories copyright ©2005-2012 
disclaimer