Huntleigh FD1-P User Manual

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Safety Aspects
2. Safety Aspects
Thhee D900-PP, D9220-PP, D9330-PP, FD22-PP, SD22-PP, MD22-PP, FD1-PP, FD33-PP, RD22 Doopplleers aandd thheeiir
proobbees aaree ddeesiigneedd too hhiighh staanddaardds oof peerfoormaanccee, reelliiaabbiilliity aandd saafeety.
Chheecckks shho
oulldd aallwaays bbee maaddee aafteer ccaarryiing oout aany reepaaiirs oor ddiismaantlliing oof thhee eeqquiipmeent.
2.1 Safety
Regular inspections must be made to check the integrity of the unit, and to ensure that the
cable is not showing any signs of wear or is noisy when flexed.
For functional testing of specific product features, refer to the user manual.
If you require any assistance with safety testing your Dopplex equipment, contact Huntleigh
Healthcare Ltd or your supplier directly.
For the U.K. refer to the Health Equipment Information Document No 95 - Code Of Practice For
Acceptance Testing Of Medical Equipment.
The following safety summary should be read before operating or carrying out any of the
procedures described in this manual.
2.2 Maintenance
2.3 Cautions
Do not use the D900-P, D920-P D930-P, FD2-P, SD2-P, MD2-P, FD1-P, FD3-P, RD2 units in the
presence of flammable gases such as anaesthetic agents.
This product is not designed for sterile use. Do not use in the sterile field unless additional
barrier precautions are taken.
Do not
- immerse in any liquid (except probe on D920-P, D930-P, FD1-P, FD3-P).
- use solvent cleaners.
- use high temperature sterilising processes (such as autoclaving).
- use E-beam or gamma radiation sterilisation.

Huntleigh FD1-P Specifications

General

Brand	Huntleigh
Model	FD1-P
Category	Medical Equipment
Language	English