Varitech

GUDID B303C0000

Usine Rotec Inc

Bariatric bed

• Primary Device ID: B303C0000
• NIH Device Record Key: 08da346a-e2b8-4f02-92cb-6eda925340e2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Varitech
• Version Model Number: Varitech
• 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	B303C0000 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-22

Devices Manufactured by Usine Rotec Inc

• B303D040 - VersaTech 1100 ULB: 2025-04-21
• B303D041 - VersaTech 1100 ULB+: 2025-04-21
• B303D042 - VersaTech 1100 ULB+: 2025-04-21
• B303E030 - VersaTech 600 ULB: 2025-04-21
• B303E031 - VersaTech 600 ULB+: 2025-04-21
• B303E040 - VersaTech 700 ULB: 2025-04-21
• B303E041 - VersaTech 700 ULB+: 2025-04-21
• B303E042 - VersaTech 700 ULB+: 2025-04-21