UNIWEB SURGICAL MASK

GUDID 04715243610140

The Surgical Mask is intended to be worn to protect both the patient and healthcare personnel from the transfer of microorganisms, body fluids and particulate material. This device is intended for adult use Only. The UNIWEB Surgical Masks are single use, disposable device, provided non-sterile.

UNIVERSAL INCORPORATION

Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use

• Primary Device ID: 04715243610140
• NIH Device Record Key: 48cfb111-0c1b-445a-a136-716ebcf0523e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UNIWEB SURGICAL MASK
• Version Model Number: ASTM Level 2
• Company DUNS: 656249554
• Company Name: UNIVERSAL INCORPORATION
• Device Count: 50
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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

Customer Support Contacts

• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw
• Phone: +886225119161
• Email: uk@uk.com.tw

Device Identifiers

Device Issuing Agency	Device ID
GS1	04715243610133 [Unit of Use]
GS1	04715243610140 [Primary]
GS1	14715243610147 [Package]; Package: 40Boxes/Carton [40 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K210513

FDA Product Code

• FXX: Mask, Surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-01-11
• Device Publish Date: 2022-01-03