Support plate

GUDID 04039361274573

Support plate

Fresenius Medical Care AG

Haemodialysis system, institutional

• Primary Device ID: 04039361274573
• NIH Device Record Key: 960ab39c-3284-4daa-a51c-5ac15e981ebb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Support plate
• Version Model Number: F50044946
• Company DUNS: 324661834
• Company Name: Fresenius Medical Care AG
• 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: false
• 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: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx
• Phone: 1 (800) 227-2572
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	04039361274573 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K243505

FDA Product Code

• KDI: Dialyzer, High Permeability With Or Without Sealed Dialysate System

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: 2025-08-11
• Device Publish Date: 2025-08-01

Devices Manufactured by Fresenius Medical Care AG

• 04039361259167 - FX CorAL: 2026-01-12 FX CorAL 60
• 04039361259587 - FX CorAL: 2026-01-12 FX CorAL 80
• 04039361259600 - FX CorAL: 2026-01-12 FX CorAL 100
• 04039361259624 - FX CorAL: 2026-01-12 FX CorAL 600
• 04039361259648 - FX CorAL: 2026-01-12 FX CorAL 800
• 04039361259662 - FX CorAL: 2026-01-12 FX CorAL 1000
• 04039361259945 - FX CorAL: 2026-01-12 FX CorAL 120
• 00840861102860 - 5008X: 2025-08-11 5008X Standard