EXPLANATION OF SYMBOLS USED
Do not use if package
is damaged or open
Do Not Resterilize
Consult Instructions
For Use
Date of Manufacture
CAUTION: Federal (US) law restricts this device
to sale / rental by or on the order of a physician.
ETL Listed, Conforms to AAMI
ES60601-1 1st edition, CSA
C22.2#60601-1 3rd edition and
IEC 60601-1 3rd edition
Refer to Instructions
For Use
Temperature
Limitations
No Bathing or
Showering
Method of
Sterilization -
Radiation
Always count and record number
of foam pieces used in wound.
Authorized Representative in
the European Community
Keep Dry
MR
Unsafe
Lot Number
Fragile
Manufacturer
Conforms with the Medical Device
Directive (93/42/EEC) and has been
subject to the conformity procedures
laid down in the council directive.
This product is designated for
separate collection at an appropriate
collection point. Do not dispose of as
household waste.
Ingress
Protection
Humidity
Limitations
Tripping Hazard
29
Use By
Single Use Only
Content Information
Catalog Number
Contains PHTHALATES
(SensaT.R.A.C.™ Pad
Tubing)
Type BF
Applied Part
Class II Device
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