Keystone ASP Oropharyngeal Sterile Specimen Collection Swab 5000 pcs

GUDID 00860003793787

ASP Oropharyngeal Sterile Specimen Collection Swab 5000 pcs

KEYSTONE MANUFACTURING, LLC

General-purpose absorbent tip applicator/swab, single-use General-purpose absorbent tip applicator/swab, single-use General-purpose absorbent tip applicator/swab, single-use General-purpose absorbent tip applicator/swab, single-use General-purpose absorbent tip applicator/swab, single-use General-purpose absorbent tip applicator/swab, single-use General-purpose absorbent tip applicator/swab, single-use General-purpose absorbent tip applicator/swab, single-use General-purpose absorbent tip applicator/swab, single-use

• Primary Device ID: 00860003793787
• NIH Device Record Key: 3e7743ae-7ab3-4d75-bc0d-d8d912bfb929
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Keystone ASP Oropharyngeal Sterile Specimen Collection Swab 5000 pcs
• Version Model Number: KMSWAB-ASPN-5000
• Company DUNS: 013799942
• Company Name: KEYSTONE MANUFACTURING, LLC
• 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: false
• 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	00860003793787 [Primary]

FDA Product Code

• KXG: Applicator, Absorbent Tipped, Sterile

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: 2021-08-25
• Device Publish Date: 2021-08-17

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