Husteon MeshNasal

GUDID 08800196110109

MediFab Co., Ltd

Intranasal splint, biodegradable

• Primary Device ID: 08800196110109
• NIH Device Record Key: b19d7665-f004-4f23-89bd-4281f15d6903
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Husteon MeshNasal
• Version Model Number: HMNS050-4010
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800196110109 [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: 2023-03-02
• Device Publish Date: 2023-02-22

On-Brand Devices [Husteon MeshNasal]

• 08800196110185: HMNSS100-4010
• 08800196110178: HMNSS080-4010
• 08800196110161: HMNSS050-4010
• 08800196110154: HMNSS100-3010
• 08800196110147: HMNSS080-3010
• 08800196110130: HMNSS050-3010
• 08800196110123: HMNS100-4010
• 08800196110116: HMNS080-4010
• 08800196110109: HMNS050-4010
• 08800196110093: HMNS100-3010
• 08800196110086: HMNS080-3010
• 08800196110079: HMNS050-3010
• 08800196110062: HMN100-4010
• 08800196110055: HMN080-4010
• 08800196110048: HMN050-4010
• 08800196110031: HMN100-3010
• 08800196110024: HMN080-3010
• 08800196110017: HMN050-3010
• 08800196110000: HMN015-2015
• 08800196100803: HMNSS050-4010