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

Devices Manufactured by STERIS CORPORATION

• 00724995225087 - NA: 2024-11-15 LED202 IN CEILING SINGLE LIGHTING SYSTEM
• 00724995225094 - NA: 2024-11-15 LED202 IN CEILING DUAL LIGHTING SYSTEM
• 00724995201876 - STERIS: 2024-10-28 STERIS 4095 SP TABLE 120V SS with Velcro attachment and 2-inch TLT Pads
• 00724995228156 - NA: 2024-10-28 2 inch TLT Pads for 7000 series Split Legs Velcro concave
• 00724995228170 - NA: 2024-10-28 3 inch TLT Pads for 7000 series Split Legs Velcro concave
• 00724995228187 - NA: 2024-10-28 3 inch TLT Pads for 7000 series Split Legs Velcro flat
• 00724995228194 - NA: 2024-10-28 4 inch TLT Pads for 7000 series Split Legs Velcro concave
• 00724995228200 - NA: 2024-10-28 4 inch TLT Pads for 7000 series Split Legs Velcro flat