QUEEN'S BENCH DIVISION
DIVISIONAL COURT
Strand London WC2A 2LL |
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B e f o r e :
MR JUSTICE CRANSTON
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COXON | Claimant | |
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MANCHESTER CITY MAGISTRATES COURT | Defendant |
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MR S BIGGS (instructed by CPS MANCHESTER) appeared on behalf of the Defendant
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Crown Copyright ©
Introduction
This case constitutes a challenge to one of the devices used to measure the level of alcohol in the breath of drivers. The device involved is a Lion Intoximeter 6000 UK, with software version 2.34, connected with the LIBIS computer system. That connection is for the purposes of keying in the details of the person being breathalysed and receiving the results from the intoxilyser. The claimant contends that the device does not have the requisite type approval. His claim is by way of judicial review of the refusal of the District Judge to state a case for consideration by this court. Permission to apply for judicial review was granted by Laws LJ and McCombe J late last year.
Background
"In the light of their being no direct evidence that the Lion Intoxilyser 6000 was altered so significantly as a result of the LIBIS connection, and bearing in mind Dr Mundy's "speculation" on this point referred to above, the judge found as a matter of fact that the device had not been taken outside of the scope of the type approval, and was an approved device."
"In the circumstances and in the light of the evidence given, I concluded it was pure speculation that the intoxilyser device was unreliable and had been altered in such a way and to such an extent that it was taken outside the scope of its type approval."
The Law
"The device known as the Lion Intoxilyser 6000 UK, manufactured by Lion Laboratories Limited composed of the Lion Intoxilyser 6000 UK, the Lion Intoxilyser UK gas delivery system type A, B or C, and software version 2.33 or 2.34."
"It does not follow that from every modification to an Intoximeter takes it out of approval, far from it. The alteration must be such in my judgment that the description in the schedule of the order no longer applies to it."
"[If] for example the Intoximeter EC/IR had no gas delivery system or had significantly different software version it would not be an approved device under the Schedule of the Approval. But there must be room to make sensible modifications without having to seek a new approval every time this is done. The test must be whether the description in the schedule still properly applies. If it does not, then the device is no longer an approved device; but if the description does still properly apply to the device it will remain an approved device even though modifications or alterations have been made. Thus the removal of one cylinder, which did not affect the operation of the device, did not take it out of the Approval. Nor in my judgment, would the supply of a device with a manual change-over valve, rather than an automatic change-over valve when the machine had two cylinders, render it no longer an approved device. It remained an Intoximeter EC/IR with a gas deliver system."
Sedley LJ agreed.
The claimant's case
Conclusion.