EN-52
DRAFT
Classications
Warning This equipment is not suitable for use in the presence
of a ammable anesthetic mixture with air, oxygen, or
nitrous oxide.
• Class I equipment
• Type BF applied part
• Degree of protection against harmful ingress of water
• Generator: IEC 60601-2-2: Requirement per clause 44.3
• Probe: IEC 60601-2-2: Requirement per clause 44.6
• Footswitch: IEC 60601-2-2: Requirement per clause 44.6,
IPX7 Water-tight Equipment
Approvals
Complies with medical safety standards:
• IEC 60601-1: 1998 + A1:1991 + A2:1995
• AS 3200.1.0: 1998
• IEC 60601-1-2: 2001
• IEC 60601-2-2: 2006
• UL 60601-1: 2003
• CSA C22.2 No. 601-1-M90
Federal Communications Commission (FCC)
FCC ID: SSH-XFC2
Trade Name: Crossre2 Console
Type or Model: 0475100000
This device complies with Part 15 of the FCC rules. Operation is subject to
the following two conditions:
1. this device may not cause harmful interference, and
2. this device must accept any interference received, including
interference that may cause undesired operation.
Note: FCC regulations provide that changes or modications not expressly
approved by Stryker Endoscopy could void your authority to operate this
equipment.
Frequency of transmission: 13.56MHz
Type of frequency / characteristics of the modulation: 10% ASK
Subcarrier: 423.75kHz, Manchester coding
Eective radiated power: 50μW
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