Fluke Biomedical 601PRO XL - Manual (Page 107)

D E V I C E R E C O R D S
6 - 5
4. Device Information Record: Definition of Fields
Field Name Maximum Characters
CONTROL#: (15)**
PROCEDURE ID: (20)**
LOCATION: (30)**
DEVICE
TYPE: (20)**
MANUFACTURER: (25)**
SERIAL
#: (16)**
TECHNICIAN: Empty field (was 5)*
DATE OF LAST TEST: Empty field (was 8)*
CLASS: (2)**
TYPE: (2)**
TEST STANDARD: (10)**
601-PRO SERIAL#: Empty field (was 15)*
LEADS: (1)**
LEAD1 AP: (5)**
LEAD1 TYPE: (2)**
LEAD2 AP: (5)**
LEAD2 TYPE: (2)**
LEAD3 AP: (5)**
LEAD3 TYPE: (2)**
LEAD4 AP: (5)**
LEAD4 TYPE: (2)**
LEAD5 AP: (5)**
LEAD5 TYPE: (2)**
POWER OFF DELAY: (3)**
STARTUP DELAY: (3)**
APPLIED CURRENT: (2)**
*These fields are present for compatibility with older versions of the
601PRO; and when received by the 601PRO Series
XL
, they are ignored. The
601PRO transmits them as empty fields.
**Restrictions, interpretation, and defaults for these fields are described
below:
⇒ Incoming device information records are checked for errors as
follows: The order, number, and size of each field and record are
fixed.
⇒ The Control Number must contain at least one character. The Test
Standard must contain a valid entry. All other fields may be empty.
⇒ Valid Classes are I, (space)I, II, or IP.
⇒ Valid Types and Lead Types are B, BF, CF, T and F.