xevonta 7204402

GUDID 04046963926182

XEVONTA DIALYZER HI 15 US, GAMMA

B.Braun Avitum AG

Hollow-fibre haemodialysis dialyser, single-use

• Primary Device ID: 04046963926182
• NIH Device Record Key: f67121c8-4d44-44cf-8d7e-5394d938b26b
• Commercial Distribution Discontinuation: 2019-02-09
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: xevonta
• Version Model Number: 7204402
• Catalog Number: 7204402
• Company DUNS: 343689704
• Company Name: B.Braun Avitum AG
• Device Count: 20
• 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: true
• 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)227-2862
• Email: BBMUS_Service.EmailOrders@bbraun.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046963926175 [Unit of Use]
GS1	04046963926182 [Primary]

FDA Product Code

• KDI: Dialyzer, high permeability with or without sealed dialysate system

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-03-03
• Device Publish Date: 2016-08-19

On-Brand Devices [xevonta]

• 04046963926304: XEVONTA DIALYZER HI 23 US, GAMMA
• 04046963926267: XEVONTA DIALYZER HI 20 US, GAMMA
• 04046963926229: XEVONTA DIALYZER HI 18 US, GAMMA
• 04046963926182: XEVONTA DIALYZER HI 15 US, GAMMA
• 04046963926144: XEVONTA DIALYZER HI 12 US, GAMMA