Hand Armor GDLPF101M

GUDID 10787081114334

LATEX HIGH RISK POWDER FREE GLOVES 13 MIL BLUE, 10/50, MED

TRANZONIC COMPANIES, THE

Hevea-latex examination/treatment glove, non-powdered, non-sterile Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 10787081114334
• NIH Device Record Key: 00b0e0e0-2dbc-4ff7-8804-885671b04741
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hand Armor
• Version Model Number: GDLPF101M
• Catalog Number: GDLPF101M
• Company DUNS: 007900020
• Company Name: TRANZONIC COMPANIES, THE
• Device Count: 50
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com
• Phone: 8003219832
• Email: info@hospeco.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00787081114337 [Primary]
GS1	10787081114334 [Package]; Contains: 00787081114337; Package: box [10 Units]; In Commercial Distribution
GS1	70787081114336 [Unit of Use]

FDA Product Code

• LYY: Latex Patient Examination Glove

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: 2020-04-28
• Device Publish Date: 2020-04-20

On-Brand Devices [Hand Armor]

• 10787081114365: LATEX HIGH RISK POWDER FREE GLOVES 13 MIL BLUE, 10/50, XXL
• 10787081114358: LATEX HIGH RISK POWDER FREE GLOVES 13 MIL BLUE, 10/50, XLG
• 10787081114334: LATEX HIGH RISK POWDER FREE GLOVES 13 MIL BLUE, 10/50, MED
• 10744897084404: LATEX HIGH RISK POWDER FREE GLOVES 13 MIL BLUE, 10/50, SM