BF00237

GUDID 00724995229283

7000-Series Split Leg Positioners without Pads, Pair, Velcro

STERIS CORPORATION

Leg procedure positioner

• Primary Device ID: 00724995229283
• NIH Device Record Key: a9a50339-d06a-4dcd-805d-5e6ec98dc21c
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 7000 Series Leg Section
• Catalog Number: BF00237
• 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
• 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	00724995229283 [Primary]

FDA Product Code

• FQO: Table, operating-room, ac-powered

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: 2024-10-28
• Device Publish Date: 2024-10-18

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• 00724995153748 - Amsco: 2026-02-23 Warming Cabinet Standard Solid Dual 24-inch 230V
• 00724995153755 - Amsco: 2026-02-23 Warming Cabinet Standard Glass Single 18-inch 230V
• 00724995153762 - Amsco: 2026-02-23 Warming Cabinet Standard Glass Dual 18-inch 230V
• 00724995153786 - Amsco: 2026-02-23 Warming Cabinet Standard Glass Single 24-inch 230V
• 00724995153793 - Amsco: 2026-02-23 Warming Cabinet Pre Glass Dual 24-inch 230V Mobile EDL EDR
• 00724995153809 - Amsco: 2026-02-23 Warming Cabinet Standard Glass Dual 24-inch 230V