Transport swab 101x16.5mm 80.625

GUDID 04038917165280

Sarstedt Aktiengesellschaft & Co.KG

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: 04038917165280
• NIH Device Record Key: 5cd30586-c366-4e38-a77b-667dbc2832fd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Transport swab 101x16.5mm
• Version Model Number: 80.625
• Catalog Number: 80.625
• Company DUNS: 388000270
• Company Name: Sarstedt Aktiengesellschaft & Co.KG
• Device Count: 500
• DM Exempt: true
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04038917083003 [Primary]
GS1	04038917165280 [Unit of Use]

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: 2022-12-08
• Device Publish Date: 2022-11-30

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