Thermoplastic

GUDID 10628341930380

Thermoplastic Immobilization Mask

CDR Systems Inc

Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material

• Primary Device ID: 10628341930380
• NIH Device Record Key: ceb9601f-d3ac-44c4-919d-f8945ad7f2cd
• Commercial Distribution Discontinuation: 2023-12-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Thermoplastic
• Version Model Number: 1
• Company DUNS: 206950904
• Company Name: CDR Systems Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca
• Phone: 403-850-7035
• Email: info@cdrsys.ca

Device Identifiers

Device Issuing Agency	Device ID
GS1	00628341930383 [Primary]
GS1	10628341930380 [Package]; Contains: 00628341930383; Package: [1 Units]; Discontinued: 2023-12-31; Not in Commercial Distribution

FDA Product Code

• IYE: Accelerator, Linear, Medical

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: 2024-01-08
• Device Publish Date: 2023-12-31

On-Brand Devices [Thermoplastic]

• 10628341930229: Thermoplastic Immobilization Materials
• 10628341930380: Thermoplastic Immobilization Mask
• 10628341930373: Thermoplastic Immobilization Materials