User Manual
CONFIDENTIAL AND PROPRIETARY – Intuitive Surgical Inc.
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DOCUMENT: 818385-01
REVISION: C
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TITLE: Installation Instructions for RFID
Module ACCRX01
The module will be used with the host device (model PS4000) and as such, required
testing and approval is completed. Use with any other host device may or may not
require additional testing and approval. Consult Hardware Compliance Engineering for
assistance.
The RFID module (Model: ACCRX01) includes the main block (P/N 318215), the top
plate (P/N 318216), the ACCR PCA (P/N 353240-06), ACCRA PCA (P/N 343460-05),
the pod support (P/N 318273), and board support (P/N 318230).
The module will be labeled to identify FCC ID (2AAZF-ACCRX01), IC ID (11508A-
ACCRX01), and Model (ACCRX01). The label is P/N 510196-01, having white
background with black text, and must be attached in a manner such that it will remain
fastened to the device during the expected life of the product. The “minimum size and
font” is that the text must be legible. Label will be applied on the main carriage block
near the ACCR location. It will not be visible when installed on host location. This is
acceptable because the approval ID information will be marked on the rear vent panel of
the host device.
The intentional radiator symbol will be included with the approval ID information (refer to
880175-02) on the host device, as required per EN60601-1-2. This marking will be
readily visible to the user of the host device without the use of tools.
Note: Statements below that are within quotation marks have fixed wording.
FCC
The host product must be labeled with the following:
“Contains FCC ID: 2AAZF-ACCRX01”
The host product manual must include following statements:
“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.”
Changes or modifications, not expressly approved by Intuitive Surgical, may void
the user‟s authority to operate the equipment. (Note: the wording for this
statement is not fixed)