General Information; Device Description - Anspach eMax 2 Plus Manual Del Usuario

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General Information

Device Description

Basket, insert and lid that securely hold Anspach devices while being processed
by hospital manual and/or mechanical/automated cleaning and sterilization
procedures.
Indications For Use
Intended to securely hold a variety of instruments while being processed by
hospital manual and/or automated washing and sterilization procedures.
Mechanical/Automated Cleaning Guidelines
Anspach devices can only be mechanically cleaned under the following
conditions:
• Cannulations must be pre-cleaned with appropriate brushes as described in
pre-cleaning instructions.
• Devices must not be cleaned using ultrasonic equipment.
• Handpieces must not be immersed in cleaning solution but may be sprayed
with it.
• Fully demineralized (deionized, distilled, or purified) water must be used
during final rinse to prevent corrosion and spots.
• Devices must be cleaned immediately after use to ensure blood and tissue
never dry on them.
• National regulations must be observed.
• You must follow standard hospital procedures.
• You must follow manufacturer's recommendations for any detergents,
disinfectants and washing equipment used.
List of Devices
Warning: Do not use to reprocess dissection tools. Dissection tools are
disposable and SINGLE USE ONLY.
Caution:
• Do not use to reprocess any devices not listed in Table 1.
• Do not reprocess the following Anspach devices in a mechanical/automated
cleaner.
• AutoLube Foot Controls
• Electric System Consoles and Foot Controls
• iMRI System and Foot Control
• Powered Irrigation Pump (IRR-PUMP-II)
Table 1
Device Catalog Number
EMAX2PLUS or XMAX
SHORT
SHORT-HD
MEDIUM
MEDIUM-HD
LONG
LONG-HD
MIA16
*MA-10S, MA-10C, MA-15S, MA-15C, MA-15ST, MA-19ST
2
Qty. Device Catalog Number Qty.
1 QD8
2 QD11
1 MA-D20
1 MA Bearing Sleeves*
1 CRANI-P
1 CRANI-A
1 CRANI-L
1 CSR60
1
1
1
2
1
1
1
1