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Brocade ISO Certificate
Cisco ISO Certificate
APC ISO Certificate
EMC ISO Certificate
AeroHive ISO
Palo Alto ISO
Palo Alto ISO Certificate #2
Oberon ISO
April 16, 2015
Oberon1315 S. Allen St, Ste 410 State College, PA 16801
QUALITY MANAGEMENT SYSTEM – ISO 9001: 2008
This letter is to verify that Accrotool, Inc holds Certificate No. 12‐1825R and operates a Quality Management System which complies with the requirements of ISO 9001:2008. All of Oberon’s products are manufactured at this location.
Best Regards, Eric M. Morgan C.O.O.
Eaton ISO
F5 ISO
Infoblox Authorization
Moxa Authorization & ISO
HatchMed authorization and ISO
StayOnline Authorization and ISO Certificate
Pure Vendor Authorization
UniTrends ISO Certificate
12018 Sunrise Valley Dr, Suite 150 RESTON, VIRGINIA 20191 Phone: +1 571 267 2999 E-Mail: [email protected] Web: www.aviziatech.com
MANUFACTURER’S AUTHORIZATION FORM
Date: July 31, 2017
To: Whom It May Concern
Subject: Avizia Resale Authorization-Venture Technologies, Birmingham, AL 35244
Avizia, Inc, a corporation organized under the laws of Delaware, United States of America (USA), having a place of business at 12018 Sunrise Valley Drive, Suite 315, Reston, VA, USA, who is a provider of technology products and services, hereby confirms that, as of the date of this letter, Venture Technologies is an authorized reseller of Avizia and is in good standing with Avizia. Avizia will, within the scope of its agreement with its authorized channels, provide support and product warranty services for Avizia products obtained through its authorized channels. This Authorization is provided for informational purposes only and must not be considered as a recommendation in favour of any party. If you need additional information, please contact Noreen Powell at +1.703-403-5216, [email protected]. Best regards, Noreen Powell Director of Avizia Channel Sales Avizia, Inc.
Certificate of Registration
This is to certify that the quality management system of
has been assessed and registered by Intertek, a CMDCAS recognized registrar, as conforming to the requirements of
ISO 13485:2003
The quality management system is applicable to
In the issuance of this certificate, Intertek assumes no liability to any party other than to the Client, and then only in accordance with the agreed upon Certification Agreement. This certificate’s validity is subject to the organization maintaining their system in accordance with Intertek’s requirements for systems certification. Validity may be confirmed via email at [email protected] or by scanning the code to the right with a smartphone. The certificate remains the property of Intertek, to whom it must be returned upon request. CT-CMDCAS-SCC-EN-LT-L-4.jan.12
Calin Moldovean, President Intertek Testing Services NA, Ltd. – Lachine, QC, Canada
JEDMED Instrument Company Main Site: 5416 JEDMED Court, St. Louis, Missouri, 63129, USA
Design and manufacture of: cabinets, chairs, stools, microscopes, video documentation equipment, endoscopes, drill system accessories, aspiration equipment, sterile manual ophthalmic trephines/donor punches, manual instruments including surgical/diagnostic/dental, fiber optic light sources and carriers, headlights, mirror warmers, ocular pressure devices, examination lights and various accessories associated with the above devices. Distribution of: microscopes, video documentation equipment, endoscopes, drill systems, sterile lacrimal intubations, fiber optic light sources and carriers, headlights, sterile tympanostomy tubes and instruments, sterile eyelid weights, mirror warmers, eye shields, corneal shields, sterile ophthalmic cannulas/needles, sterile wound dressings, medicament bottles, IV poles, stainless steel ware/instrument trays/cotton jars and various accessories associated with the above devices.
Certificate Number: 9425-5 Initial Certification Date: 11 May 2010 Certificate Effective Date: 11 May 2013 Certificate Expiry Date: 11 May 2016
)
REGI STRATION CERTIF ICATE
Thls document certifles thot the odministrotion systems ofMendtronix, lnc.
55 Ray Hill Drive, Suite A, Latrobe, Pennsyluania 15650I j880 Stowe Drive, Poway, California 92064
I l5 Smokehill Lane, Woodstock, Georgia 30188hove been ossessed ond opproved by QAS lnternotlonol
to the following manogement systems, stondords ond guldelines:
ISO 9001 : 2008With the permitted exclusion of clause 7. j Design and Development
The approved administrotion systems opply to the following:
The provision for Seruicing and Logistic Support of Audio Visual Equipment.
Original Approval
Current Certificate
Certificate Expiry
2Eh October2ol3
28h octobet 2013
28h october2ol4
Certif icateNumber,._.......A5_A1.7_/.AS..AA1_B_/..U..5.3_A19.....
This certificale remarns vald whrle the holder maintains lherr qualrty administration systems in
accordance with lhe standards and gurdelrnes slated above, whrch will be audited annually by
QAS lnlernational The holder is entitled to display lhe above regrstratron mark for the duration
of this certificate vvtrich should be relurned to QAS lntemationalupon reasonable request
lssuing Office: OAS lnternational 20A Oxford Street, Malmesbury, Wiltshire SN16 gAx, UK
On behalf of QAS
QAS lnternational
Accredited Body: UL DQS Inc., 1130 West Lake Cook Road, Suite 340, Buffalo Grove, IL 60089 USA
CERTIFICATE
This is to certify that
Modo, Inc.
20325 NW von Neumann #170 Beaverton, OR 97006 United States of America
has implemented and maintains a Quality Management System.
Scope: The design of custom medical carts and furniture and the control and management of manufacturing and logistics.
Through an audit, documented in a report, it was verified that the management system fulfills the requirements of the following standard:
ISO 9001 : 2008
Certificate registration no.
Date of original certification
Date of certification
Valid until
10009378 QM08
2009-12-16
2012-12-16
2015-12-15
UL DQS Inc.
Ganesh Rao Managing Director
12018 Sunrise Valley Dr., Ste. 315 Reston, Virginia 20191 Phone: +1 703 973 0454 Web: www.avizia.com
P a g e | 1
Quality Policy
Avizia is committed to consistently satisfying the needs and expectations of our customers by delivering innovative solutions built to standards that guarantee their quality.
This high level of quality is achieved through the development of purpose-build telemedicine devices, a thorough implementation process, and best-in-class customer support. In addition, Avizia maintains a quality system that complies with:
• ISO 13485 • Health Canada MDR • MDD/AIMD/IVDD • US FDA Quality System Requirements
Avizia is committed to maintaining the effectiveness of the quality management system to meet or exceed all applicable regulations and standards.
Safety Policy
Avizia is committed to delivering products that are safe to use by healthcare providers and their patients in accordance to the included Instructions for Use. The company’s products meet or exceed regulatory requirements and follow industry best practices.
Avizia also provides a safe, clean work environment for employees, and maintains safety processes that conform to national and international requirements.
Product Quality
CA750 Telemedicine Cart
• Meets all of the published specifications • Is registered with the US FDA as a Class I Medical Device (3010402749) • Meets the Quality System Requirements of the FDA 21 CFR 820, the Health Canada
MDR and the MDD/AIMD/IVDD • Is certified to the IEC 60601 Electrical Safety Standard • Is produced within the Avizia Quality Management System that complies with ISO 13485 • Is manufactured in Avizia’s ISO 9001:2008 certified production facility (US3618)
CA300/CA310 Telemedicine Cart
• Meets all of the published specifications • Is registered with the US FDA as a Class I Medical Device (3010402749) • Meets the Quality System Requirements of the FDA 21 CFR 820, the Health Canada
MDR and the MDD/AIMD/IVDD • Is certified to the IEC 60601 Electrical Safety Standard • Is produced within the Avizia Quality Management System that complies with ISO 13485 • Is manufactured in Avizia’s ISO 9001:2008 certified production facility (US3618)
