Keystone Nasal / Respiratory Specimen Collection Kit – 100 pack

GUDID 00860005748310

Nasal / Respiratory Specimen Collection Kit – 100 pack

KEYSTONE MANUFACTURING, LLC

General tissue specimen container IVD, saline General tissue specimen container IVD, saline General tissue specimen container IVD, saline General tissue specimen container IVD, saline General tissue specimen container IVD, saline General tissue specimen container IVD, saline General tissue specimen container IVD, saline General tissue specimen container IVD, saline General tissue specimen container IVD, saline General tissue specimen container IVD, fixative/saline General tissue specimen container IVD, fixative/saline General tissue specimen container IVD, fixative/saline General tissue specimen container IVD, fixative/saline General tissue specimen container IVD, fixative/saline General tissue specimen container IVD, fixative/saline General tissue specimen container IVD, fixative/saline General tissue specimen container IVD, fixative/saline

• Primary Device ID: 00860005748310
• NIH Device Record Key: 635f35af-8f6c-4fea-8a76-6047f55e3a30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Keystone Nasal / Respiratory Specimen Collection Kit – 100 pack
• Version Model Number: KMSVKIT-KM05-100
• 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	00860005748310 [Primary]

FDA Product Code

• JSG: Culture Media, Non-Selective And Non-Differential

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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