BF683

GUDID 00724995185312

The Wide Wedge Sacral Rest provides positioning and Support to the Sacral area.

STERIS CORPORATION

Torso intraoperative positioner

• Primary Device ID: 00724995185312
• NIH Device Record Key: d4c5c831-50ae-40a7-84d1-3ecd5b24260a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: BF683
• Catalog Number: BF683
• 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
• 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	00724995185312 [Primary]

FDA Product Code

• CCX: SUPPORT, PATIENT POSITION

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: 2021-05-03
• Device Publish Date: 2021-04-23

Devices Manufactured by STERIS CORPORATION

• 00724995153724 - Amsco: 2026-02-23 Warming Cabinet Standard Solid Single 24-inch 230V
• 00724995153731 - Amsco: 2026-02-23 Warming Cabinet Standard Solid Dual 24-inch 230V Mobile
• 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