MIETHKE proGAV 2.0 XABO Instrucciones De Manejo página 36

| INSTRUCTIONS FOR USE
EU conformity marking,
xxxx indicates the identifier of the
responsible notified body
Medical device
Manufacturer
Date of manufacture
Use-by date
Batch code
Catalogue number
Serial number
Sterilised using irradiation
Do not resterilise
Do not reuse
Do not use if package is damaged and
consult instructions for use
Keep dry
Upper limit of temperature
Keep away from sunlight
Consult instructions for use / electronic
instructions for use
Caution
Contains a medical substance
36
Non-pyrogenic
Free of natural rubber latex, latex-free
Indicates that in the USA, the product
may only be issued to physicians.
MR Conditional
Patient identification
Date
Healthcare centre or doctor
Patient information website
Model number / European Medical
Device Nomenclature Code
In compliance with regulatory requirements,
Christoph Miethke GmbH & Co. KG has nomi-
nated medical device consultants as contacts
for all product-related questions.
You can contact our medical device consul-
tants at:
proGAV ® 2.0 XABO ®