Single Use Aspiration Needle N5432340

GUDID 14953170458382

OLYMPUS MEDICAL SYSTEMS CORP.

General-purpose endoscopic needle, single-use

• Primary Device ID: 14953170458382
• NIH Device Record Key: a7bbddb9-68fd-4f23-95fe-77fa54105f25
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Single Use Aspiration Needle
• Version Model Number: NA-201SX-4022
• Catalog Number: N5432340
• Company DUNS: 711789789
• Company Name: OLYMPUS MEDICAL SYSTEMS CORP.
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx
• Phone: +1(800)401-1086
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	04953170458385 [Primary]
GS1	14953170458382 [Package]; Contains: 04953170458385; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• KTI: Bronchoscope Accessory

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: 2025-08-22
• Device Publish Date: 2025-08-14

On-Brand Devices [Single Use Aspiration Needle]

• 14953170169974: SINGLE USE ASPIRATION NEEDLE
• 14953170169967: NA-200H-8022
• 14953170458405: NA-201SX-4022
• 14953170458399: NA-201SX-4022
• 14953170458382: NA-201SX-4022