Bird Sentry™ Blender
L1383 Rev. D
v
EMC Notice
This equipment generates, uses, and can radiate radio frequency energy If not installed and used in
accordance with the instructions in this manual, electromagnetic interference may result. The
equipment has been tested and found to comply with the limits set forth in IEC 601-1-2 for
Medical Products. These limits provide reasonable protection against electromagnetic interference
when operated in the intended use environments described in this manual.
MRI Notice
This equipment contains electromagnetic components whose operation can be affected by intense
electromagnetic fields.
Do not operate the Bird Sentry blender unattended in an MRI environment or in the vicinity of high-
frequency surgical diathermy equipment, defibrillators, or shortwave therapy equipment.
Electromagnetic interference could disrupt the operation of the Bird Sentry blender.
Regulatory Notice
Federal law restricts the sale of this device except by and on order of a physician.
Declaration of Conformity Notice
This medical equipment complies with the Medical Device Directive, 93/42/EEC, and the following
Technical Standards, to which Conformity is declared:
IEC 601-1-2
IEC 601-1-2: 1993
ISO 9001: 1994
EN 46001, MDD-Annex-II
Type of Equipment: Medical Equipment, O
2
Blender/Monitor
Trade name: Bird Sentry
Model No.: 15625 Series
If you have any questions regarding the Declaration of Conformity for this product, please contact
CareFusion Corporation.
