BF386

GUDID 00724995163921

The HLT Pad Head Section is used with the STERIS Cmax, 4085 and 5085 General Surgical Table.

STERIS CORPORATION

Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion Multifunction body cushion

• Primary Device ID: 00724995163921
• NIH Device Record Key: 59c4bf70-c35c-4fa0-83a8-ba6c59c5f395
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: Table Pad
• Catalog Number: BF386
• 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	00724995163921 [Primary]

FDA Product Code

• LWG: SURGICAL TABLE CUSHION

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: 2021-04-12
• Device Publish Date: 2021-04-02

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