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MN1-5752
Rev.8
Label 2
Label 3
(Examples)
This instrument complies with Directive 93/42/EEC
relating to Medical Device and Directive 2011/65/EU
relating to RoHS.
IPX7
IPX7 mark
See section 2-2, "Specifications".
Type BF applied part
Do not waste the equipment as general waste.
Comply with a local regulation.
See section 10.
STERRAD sterilization compatibility mark
See section 5.
Safety warning sign
Biohazard
See section 5.
Follow the instruction manual to operate this equipment.
If not avoided, may result in injury, property damage, or the
equipment trouble.
Country of manufacture:
JAPAN or CHINA
Model
Serial No.
Manufacturer
Address
Rx Only:
By prescription only. U.S. Federal Law
restricts this device to sale on order of a
physician only.
-6-
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