This Combined Synopsis/Solicitation opportunity from Department Of Defense was posted on May 22, 2014. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

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SORIN S5 Heart Lung Bypass Unit

Closed

N6264514RCES037Federal

Submission Closed06/03/2014, 03:00:00 PM UTC

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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NAICS: 339112

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MEDICAL SUPPLY CHAIIN FSH

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General Info

Agency

Department Of Defense → Naval Medical Logistics Command

NAICS

339112 - Surgical and Medical Instrument Manufacturing

Place of Performance

Ft Detrick, Ft Detrick, MD, 21701, USA

Set-Aside

NONE

Documents

SORIN_combined_sysnopsis.doc

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Timeline

PhaseClosed

PostedMay 15

Presolicitation

Type ChangedMay 22

Presolicitation → Combined Synopsis

Response DeadlineJun 3

Deadline has passed

Submission Closed

06/03/2014, 03:00:00 PM UTC

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Organization & Contact Information

AgencyDepartment Of Defense → Naval Medical Logistics Command

Contacts2 people available

OfficeFORT DETRICK, MD, 21702-9203, USA

Organization / AgencyDepartment Of Defense → Naval Medical Logistics Command

Office AddressFORT DETRICK, MD, 21702-9203, USA

Contacts

Brian D. MillerContract Specialist

contact@example.gov

+1 (555) 000-0000

Tameka N DavisContracting Officer

contact@example.gov

+1 (555) 000-0000

Full Description

Naval Medical Center Portsmouth has a requirement for two (2) heart-lung bypass units [ECRI Device code 11-969]. The systems shall be able to provide temporary external circulatory support for open heart surgery. The systems shall be able to oxygenate venous blood and pump it throughout the arterial system. This requirement is brand name or equal to a Sorin S5 Heart-Lung bypass unit with associated components as described in the component list. The systems shall be modular in design, and individual components and modules shall be able to be added and removed from the system. The systems shall have a mast system for the positioning of different accessories. The systems shall have an emergency uninterruptible power supply equipped with a manual crank. The uninterruptible power supply shall be capable of up to 90 minutes of bypass operating time depending on the workload. The systems shall have three (3) single roller pumps that are operable in continuous or pulse mode. The systems shall include one (1) centrifugal pump. The systems shall have a locking wheel/knob mechanism for inclusion adjustment to prevent accidental adjustment. The systems shall have an arterial line clamp. The systems shall have at least two pressure sensors and at least four temperature sensors. The systems shall be capable of monitoring venous saturation, hematocrit, and venous temperature. The systems shall be able to stop the connected pump when an air bubble is detected within the tubing. The systems shall have a cardioplegia sensor capable of automatic and manual operational modes. The cardioplegia sensor shall also be capable of measuring the total volume delivered from the start of the procedure. The systems shall have a level sensor capable of detecting when blood falls below acceptable levels in the unit. The systems shall have both audible and visual alarms. The systems shall have an electronic gas blender with four connectors for Air, O2, CO2, and total gas flow. The systems shall have at least three timers which can be set independently. The units shall have an attached LED lamp. The systems shall have cable holding and organizing systems and clamps to allow for proper positioning of the system during procedures. The power requirement for the heart-lung bypass units is 120VAC, 60Hz. The systems shall also include a warming/cooling unit, patient, heart-lung bypass [ECRI Device code 17-206]. The warming/cooling units shall have separate cold and warm water tanks to allow for fast changes between warm and cold cardioplegia. The warming/cooling units shall have separate water circuits for controlling the temperature of the patient and for controlling the temperature of the cardioplegia solution. The power requirement for the warming/cooling units is 120VAC, 60Hz. See attached combined synopsis/solicitation

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