HuBDIC Nasal Aspirator

GUDID 08800132210177

HuBDIC Co., Ltd.

Nasal aspirator, manual

• Primary Device ID: 08800132210177
• NIH Device Record Key: ecf1347e-7211-4315-98b0-b9d83feeb48d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HuBDIC Nasal Aspirator
• Version Model Number: HNA-20P
• Company DUNS: 688454128
• Company Name: HuBDIC 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800132210177 [Primary]

FDA Product Code

• BSY: Catheters, Suction, Tracheobronchial

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: 2022-09-15
• Device Publish Date: 2022-09-07

On-Brand Devices [HuBDIC Nasal Aspirator]

• 08800132210177: HNA-20P
• 08800132210160: HNA-20B