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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• 00724995204150 - PRO-LITE: 2025-12-24 The PRO-Lite Sterilization Tray Mat, 13-inch x 7.75-inch, is used in V-PRO Low Temperature Sterilization Systems and STERRAD NX,
• 00724995204167 - PRO-LITE: 2025-12-24 The PRO-Lite Sterilization Tray Mat, 19-inch x 7.75-inch, is used in V-PRO Low Temperature Sterilization Systems and STERRAD NX,
• 00724995204174 - PRO-LITE: 2025-12-24 The PRO-Lite Sterilization Tray Mat, 27-inch x 7.75-inch, is used in V-PRO Low Temperature Sterilization Systems and STERRAD NX,
• 50724995229554 - PRE-KLENZ: 2025-12-24 Pre-Klenz Enzymatic Soak Shield Kit is used to keep contaminated instruments moist during transportation for up to 72 hours