H&O Equipments CryoPen Series User Manual page 5

The above list of products is correct at the time of printing. Some
articles may no longer be available when reading this document.
Some articles may not be available in certain countries.
CryoPen® is the registered trademark of H&O Equipments nv/sa for
Europe, the Middle East, Africa and Asia Pacific.
EC or Canadian Declaration of Conformity is available and can be
obtained upon simple request.
CryoProbe™ is the registered trademark of H&O Equipments nv/sa
and is distributed under that name in the US and Canada.
CryoPen® and CryoProbe™ are the same instruments and are both
manufactured by H&O Equipments nv/sa.
FDA certificate is available and can be obtained upon simple request.
CryoPen and CryoProbe instruments are intended for the controlled
destruction of unwanted tissue by application of extreme cold using
liquefied N O. Pathological indications are benign skin lesions such
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as: angiofibroma, granuloma, condyloma, dermafibroma, molluscum
contagiosum, porokeratosis, seborrheic keratosis, actinic keratosis,
solar lentigo, warts on the feet, warts on the hands. This list is not
complete.
All mentioned products are manufactured in the European
Community by,
H&O Equipments nv/sa, Rue des Journaliers 1,
7822 Ghislenghien, Belgium.
Telephone : +32 68 26 86 00, Fax : +32 68 55 48 28
E-mail : info@ho-equipments.com
Website : www.ho-equipments.com
This manual's version : 120415CPEPR
Notified Body Number: 0120
Canadian License Number: 89787
The most recent version of this user manual and other language
versions can be downloaded from the manufacturer's website under
'Press & Manuals': www.ho-equipments.com
Attention! Reference is made to the liability waiver at the back of
this manual.
Used symbols
Manufacturer
Caution, consult accompanying documents
REF
Catalogue number
SN
Serial number
Notified body nr 0120 SGS UK
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