BF538

GUDID 00724995165376

The Foot Traction Boot Pads with Straps, Adult is used with the TenZor Carbon Fiber Traction Unit Assembly.

STERIS CORPORATION

Traction boot Traction boot Traction boot Traction boot Traction boot Traction boot Traction boot Traction boot Traction boot Traction boot Traction boot Traction boot Traction boot Traction boot Traction boot

• Primary Device ID: 00724995165376
• NIH Device Record Key: a1bca4b2-f1b2-46d3-86e6-563a59ae3796
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: BF538
• Catalog Number: BF538
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00724995165376 [Primary]

FDA Product Code

• HST: Apparatus, traction, non-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: 2021-05-03
• Device Publish Date: 2021-04-23

Devices Manufactured by STERIS CORPORATION

• 00724995225155 - NA: 2024-04-16 The Perineal Post Only, Adult provides support in the perineal area.
• 00724995225162 - NA: 2024-04-16 The Perineal Post Only, Adult, 7 inch Short provides support in the perineal area.
• 00724995228453 - VERIFY: 2024-04-03 The VERIFY Spore Test Strip for S40 Sterilant offers the ability to test sporicidal activity of the S40 use dilution within the
• 00724995229078 - NA: 2024-03-18 7080 Table Core, 110 120V, Velcro, No Pads
• 00724995229085 - NA: 2024-03-18 7080 Table Core, 110-120V, Mushroom Caps, No Pads
• 00724995229139 - NA: 2024-03-18 7080 Table, 110-120V, Velcro, Dual Articulating Head, Feather Weight Leg Section, 2-inch TLT Pads
• 00724995229160 - NA: 2024-03-18 7000-Series Single Articulating Headrest, without Pad, Velcro
• 00724995229177 - NA: 2024-03-18 7000-Series Single Articulating Headrest, with 2 inch TLT pad, Velcro