BF864

GUDID 00724995217259

The Replacement Pad Set is used with PowerLift Freedom Stirrups (pair) - Adult 500 pound is used with

STERIS CORPORATION

Heel stirrup cushion/pad

• Primary Device ID: 00724995217259
• NIH Device Record Key: 03bc269a-581c-49f6-a726-ebb0d0ca9e50
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: Stirrup Pad
• Catalog Number: BF864
• 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: true
• 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: false

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
• 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	00724995217259 [Primary]

FDA Product Code

• EYD: STIRRUPS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-08-02
• Device Publish Date: 2022-12-20

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• 00724995225148 - NA: 2025-04-08 The Adult Wedge Shaped Sacral Rest attaches to Orthopedic Extension and OrthoVision Table to support the patients Sacral area an
• 00724995232184 - NA: 2025-04-08 The Fujifilm GI Scopes Tubing and Connector Set 5 is used with the Reliance 6500 Series Endoscope Drying and Storage Cabinet.
• 00724995232191 - NA: 2025-04-08 The Pentax GI Scopes Tubing and Connector Set 2 is used with the Reliance 6500 Series Endoscope Drying and Storage Cabinet.
• 00724995232207 - NA: 2025-04-08 The Fujifilm GI Scopes Tubing and Connector Set 7 is used with the Reliance 6500 Series Endoscope Drying and Storage Cabinet.
• 00724995232214 - NA: 2025-04-08 The Fujifilm GI Scopes Tubing and Connector Set 8 is used with the Reliance 6500 Series Endoscope Drying and Storage Cabinet.
• 00724995232221 - NA: 2025-04-08 The Fujifilm GI Scopes Tubing and Connector Set 9 is used with the Reliance 6500 Series Endoscope Drying and Storage Cabinet.