IOPI MEDICAL 2.3 Manual Del Usuario página 2

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IOPI
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IOPI® Medical LLC is certified to ISO 13485:2003 under the Canadian Medical Device Regulation
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Identity
Catalogue Number
Serial Number
Manufacturing Date
Consult Instructions
Before Use
Caution
Type B patient applied
part according to IEC
60601-1
9 Volt Alkaline Battery
Do Not Dispose of in
household Refuse
EU Authorized
Representative
Manufactured By
Conformity European
Notes:
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