BF412

GUDID 00724995164515

The Cardiovascular Accessory Package is used with STERIS Surgical Tables.

STERIS CORPORATION

Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top Universal operating table top

• Primary Device ID: 00724995164515
• NIH Device Record Key: 26dbef51-0ab9-4bf7-a841-976003f47450
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: BF412
• Catalog Number: BF412
• Company DUNS: 036985604
• Company Name: STERIS CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00724995164515 [Primary]

FDA Product Code

• FQO: TABLE, OPERATING-ROOM, AC-POWERED

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-05-03
• Device Publish Date: 2021-04-23

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• 00724995217617 - NA: 2024-04-25 enspire 300 Connector Olympus Air Water Valve is used with the enspire 300 Series Automated Endoscope Reprocessor
• 00724995217624 - NA: 2024-04-25 enspire 300 Connector Olympus Suction Valve is used with the enspire 300 Series Automated Endoscope Reprocessor
• 00724995217631 - NA: 2024-04-25 enspire 300 Connector Olympus Suction Valve is used with the enspire 300 Series Automated Endoscope Reprocessor