Imperial Single Step Footstool OR-36360

GUDID 07540162040382

Footstool\16Lx12Wx8H

Imperial Surgical Ltd

Footstool Footstool Footstool Footstool Footstool Footstool Footstool Footstool Footstool Footstool Footstool Footstool Footstool Footstool Footstool Footstool

• Primary Device ID: 07540162040382
• NIH Device Record Key: 5b60d8b3-9c9d-40f2-b82f-7dc0dd58dfc6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Imperial Single Step Footstool
• Version Model Number: OR-36360
• Catalog Number: OR-36360
• Company DUNS: 245253575
• Company Name: Imperial Surgical Ltd
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07540162040382 [Primary]

FDA Product Code

• FZM: Stool, Operating-Room

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: 2023-08-07
• Device Publish Date: 2023-07-28

On-Brand Devices [Imperial Single Step Footstool]

• 07540162040405: Footstool\30Lx12Wx8H
• 07540162040399: Footstool\30Lx12Wx8H
• 07540162040382: Footstool\16Lx12Wx8H