Adult Pads – Philips FR2
CE Marked
Comply with European Directive and International Standards
(IEC/EN 60601-1, IEC/EN 60601-2- 4, ANSI/AAMI DF-80, EN ISO 10993-1)
MADE IN ITALY
The Pads are manufactured in accordance with the applicable European regulations (CE) on medical devices and meet the requirements of harmonized standards that apply to them. Regulatory requirements set by the Countries under MDSAP scheme are also applied: Australian ATGMDR 2002, Brazilian ANVISA RDC, Canadian CMDR, Japanese MHLW Ordinance no.169, U.S. FDA CFR Title 21 Part 820.
PLEASE NOTE
Unfortunately, we cannot accept returns on Defibrillator Pads and Batteries as they are Ordered from the distributor as required and have set Expiry Date.
If you need assistance, please call 0404 62111.