Husteon Nasal

GUDID 08800196100575

MediFab Co., Ltd

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• Primary Device ID: 08800196100575
• NIH Device Record Key: 551100ee-8d18-46c7-88f5-893190a9e46a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Husteon Nasal
• Version Model Number: HNS100-4010
• Company DUNS: 694603020
• Company Name: MediFab Co., Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800196100575 [Primary]

FDA Product Code

• LYA: Splint, Intranasal Septal

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: 2022-07-11
• Device Publish Date: 2022-07-01

On-Brand Devices [Husteon Nasal]

• 08800196100636: HNSS100-4010
• 08800196100629: HNSS080-4010
• 08800196100612: HNSS050-4010
• 08800196100605: HNSS100-3010
• 08800196100599: HNSS080-3010
• 08800196100582: HNSS050-3010
• 08800196100575: HNS100-4010
• 08800196100568: HNS080-4010
• 08800196100551: HNS050-4010
• 08800196100544: HNS100-3010
• 08800196100537: HNS080-3010
• 08800196100520: HNS050-3010
• 08800196100513: HN100-4010
• 08800196100506: HN080-4010
• 08800196100490: HN050-4010
• 08800196100483: HN100-3010
• 08800196100476: HN080-3010
• 08800196100469: HN050-3010