Sterile 3” Foam Swab with yellow handle V2

GUDID 00850027193366

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

Steripack (usa) Limited LLC

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

• Primary Device ID: 00850027193366
• NIH Device Record Key: 597b48f2-03ff-4ca8-878a-a1e201e1ca46
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sterile 3” Foam Swab with yellow handle V2
• Version Model Number: 60612
• Company DUNS: 042126640
• Company Name: Steripack (usa) Limited LLC
• Device Count: 1700
• 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	00850027193106 [Primary]
GS1	00850027193366 [Unit of Use]

FDA Product Code

• KXG: Applicator, Absorbent Tipped, Sterile

Sterilization

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

[00850027193366]

Radiation Sterilization

[00850027193366]

Radiation Sterilization

[00850027193366]

Radiation Sterilization

[00850027193366]

Radiation Sterilization

[00850027193366]

Radiation Sterilization

[00850027193366]

Radiation Sterilization

[00850027193366]

Radiation Sterilization

[00850027193366]

Radiation Sterilization

[00850027193366]

Radiation Sterilization

[00850027193366]

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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