VersaTech LB

GUDID B303F0100

Usine Rotec Inc

Basic electric hospital bed

• Primary Device ID: B303F0100
• NIH Device Record Key: 01cfc2a9-9a42-4731-b062-8ed9dbf51612
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VersaTech LB
• Version Model Number: VLB
• Company DUNS: 245707815
• Company Name: Usine Rotec Inc
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B303F0100 [Primary]

FDA Product Code

• FNL: Bed, Ac-Powered Adjustable Hospital

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: 2021-07-13
• Device Publish Date: 2021-07-05

Devices Manufactured by Usine Rotec Inc

• B303B0100 - MultiTech ULB: 2021-07-13
• B303D0300 - VersaTech 1100 ULB: 2021-07-13
• B303E0200 - VersaTech 600 ULB: 2021-07-13
• B303F0100 - VersaTech LB: 2021-07-13
• B303F0100 - VersaTech LB: 2021-07-13
• B303A0000 - Multitech 2.0: 2018-03-29
• B303B0000 - Multitech 8: 2018-03-29
• B303C0000 - Varitech: 2018-03-29
• B303C0100 - Varitech 2.0: 2018-03-29