BF452

GUDID 00724995165079

The Shoulder Table Chair Cups are used in conjunction with the Shoulder Table and provide stability for the head and chin during shoulder procedures.

STERIS CORPORATION

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• Primary Device ID: 00724995165079
• NIH Device Record Key: e4760f7e-f31b-430b-9556-f7810dc7c751
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: BF452
• Catalog Number: BF452
• Company DUNS: 036985604
• Company Name: STERIS CORPORATION
• Device Count: 10
• 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: true
• 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	00724995165079 [Unit of Use]
GS1	10724995165076 [Primary]

FDA Product Code

• HSS: HALTER, HEAD, TRACTION

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

Devices Manufactured by STERIS CORPORATION

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• 50724995216929 - Revital-Ox: 2024-04-25 Revital-Ox PAA HLD Solution Part A is used Revital-Ox PAA HLD Part B and the enspire 300 Series Automated Endoscope Reprocessor
• 00724995217587 - NA: 2024-04-25 enspire 300 Connector Olympus Channel Separator is used with the enspire 300 Series Automated Endoscope Reprocessor
• 00724995217594 - NA: 2024-04-25 enspire 300 Connector Olympus Channel Separator is used with the enspire 300 Series Automated Endoscope Reprocessor
• 00724995217600 - NA: 2024-04-25 enspire 300 Connector Olympus Air Water Valve is used with the enspire 300 Series Automated Endoscope Reprocessor
• 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