03BA-FO 302-10010

GUDID 00814005021485

03BA-FO

Quality Aspirators, Inc.

General-purpose light source

• Primary Device ID: 00814005021485
• NIH Device Record Key: ab415c00-6174-4d56-bfb5-7ad04d53a473
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 03BA-FO
• Version Model Number: 03BA-FO
• Catalog Number: 302-10010
• Company DUNS: 121431159
• Company Name: Quality Aspirators, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• 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	00814005021485 [Primary]

FDA Product Code

• EAY: LIGHT, FIBER OPTIC, DENTAL

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: 2025-03-07
• Device Publish Date: 2025-02-27

Devices Manufactured by Quality Aspirators, Inc.

• 00814005020006 - TA: 2025-03-07 TA
• 00814005020013 - 15P2-90A: 2025-03-07 15P2-90A
• 00814005020037 - 03BAT: 2025-03-07 03BAT
• 00814005020051 - 15P3A: 2025-03-07 15P3A
• 00814005020068 - 03BA: 2025-03-07 03BA
• 00814005020082 - 02BA: 2025-03-07 02BA
• 00814005020099 - 46P3M: 2025-03-07 46P3M
• 00814005020105 - 15P2AT: 2025-03-07 15P2AT