Ipas is committed to producing the highest-quality MVA instruments available. All Ipas MVA instruments (aspirators, cannulae and Denniston Dilators) are listed with the United States Food and Drug Administration (USFDA). Our facility is registered with the USFDA.
Ipas's quality system has been certified compliant for ISO 13485 (International Standards for Quality) by the British Standards Institute (BSI). Ipas MVA instruments were awarded the CE Mark as per the Medical Device Directive 93/42/EEC. This certification is required for sale of products in member countries of the European Union.
Ipas will replace or repair, free of charge either direct or through its distributors worldwide, any of our products which are found to be faulty by reason of poor craftsmanship or materials. This guarantee does not cover defects arising from accident, neglect or misuse.
For information about purchasing, contact:
Ipas
PO Box 5027
Chapel Hill, NC 27514 USA
phone: 800.334.8446 (toll free in USA), 919.960.6453 or 919.967.7052
fax: 919.442.0080
email: customerservice@ipas.org