Combifix™ Baseplate 151014MR

GUDID 00841439111871

Combifix™ Baseplate

MEDTEC, INC.

Radiological arm/leg positioner

• Primary Device ID: 00841439111871
• NIH Device Record Key: b2edca5e-818c-4099-85c9-7820f1100ece
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Combifix™ Baseplate
• Version Model Number: 151014MR
• Catalog Number: 151014MR
• Company DUNS: 103977526
• Company Name: MEDTEC, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439111871 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K060737

FDA Product Code

• IYE: Accelerator, linear, medical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-05-31
• Device Publish Date: 2018-08-20

On-Brand Devices [Combifix™ Baseplate]

• 00841439111871: Combifix™ Baseplate
• 00841439100820: Combifix™ Baseplate