nextaro® va

GUDID 04063574100022

nextaro® va (with 15µm filter, nominal for a 20mm vial)

sfm medical devices GmbH

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• Primary Device ID: 04063574100022
• NIH Device Record Key: 05db9839-f9cf-47bf-bbb6-7b11b326cc04
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: nextaro® va
• Version Model Number: 10002
• Company DUNS: 315549311
• Company Name: sfm medical devices GmbH
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04063574100022 [Primary]

FDA Product Code

• LHI: Set, I.V. Fluid Transfer

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-10-01
• Device Publish Date: 2021-09-23

On-Brand Devices [nextaro® va]

• 04063574100022: nextaro® va (with 15µm filter, nominal for a 20mm vial)
• 04063574200296: nextaro® va (with 15µm filter, nominal for a 20mm vial)