TraumaTherm

GUDID 05060195340898

TCU203 Control Unit

INSPIRATION HEALTHCARE GROUP PLC

Electric pad whole-body heating system

• Primary Device ID: 05060195340898
• NIH Device Record Key: 629906e5-4f6f-4cb5-a15a-e950ae6a7b9a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TraumaTherm
• Version Model Number: TCU203
• Company DUNS: 235903494
• Company Name: INSPIRATION HEALTHCARE GROUP PLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +441709361000
• Email: info@inspiration-healthcare.co

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060195340898 [Primary]

FDA Product Code

• DWJ: System, thermal regulating

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-11-04

On-Brand Devices [TraumaTherm]

• 05060195340911: TCU205 Control Unit
• 05060195340904: TCU204 Control Unit
• 05060195340898: TCU203 Control Unit
• 05060195340881: TCU202 Control Unit
• 05060195340874: TCU201 Control Unit
• 05060195340867: TCU200 Control Unit
• 05060195340775: TTM-SPE Mattress
• 05060195340768: TTM3 Mattress
• 05060195340751: TTM2 Mattress
• 05060195340744: TTM1 Mattress