Sterile Narrow Polyester Spun Swab

GUDID 00850027193212

single use, sterile pouched polyester spun swabs for specimen ciollection sampling from nasal area, i.e. Anterior nares

Steripack (usa) Limited LLC

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• Primary Device ID: 00850027193212
• NIH Device Record Key: 449effc0-ba43-4701-8429-9f1ac3a95d06
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sterile Narrow Polyester Spun Swab
• Version Model Number: 60567
• Company DUNS: 042126640
• Company Name: Steripack (usa) Limited LLC
• Device Count: 2000
• 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: true
• Expiration Date: true
• 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	00850027193212 [Unit of Use]
GS1	00860004112723 [Primary]

FDA Product Code

• KXG: Applicator, Absorbent Tipped, Sterile

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[00850027193212]

Radiation Sterilization

[00850027193212]

Radiation Sterilization

[00850027193212]

Radiation Sterilization

[00850027193212]

Radiation Sterilization

[00850027193212]

Radiation Sterilization

[00850027193212]

Radiation Sterilization

[00850027193212]

Radiation Sterilization

[00850027193212]

Radiation Sterilization

[00850027193212]

Radiation Sterilization

[00850027193212]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-11
• Device Publish Date: 2022-10-03

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