HALYARD SGL96090

GUDID 20680651200901

HALYARD SGL96090 Polyisoprene Textured Size (9.0), Powder-Free Polyisoprene Surgical Glove

Ansell

Polyisoprene surgical glove, non-powdered, non-antimicrobial

• Primary Device ID: 20680651200901
• NIH Device Record Key: e0487e9e-6b4f-4de2-9155-331028315587
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HALYARD
• Version Model Number: SGL96090
• Catalog Number: SGL96090
• Company DUNS: 120522524
• Company Name: Ansell
• Device Count: 1
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com
• Phone: 775-470-7106
• Email: don.cronk@ansell.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10680651200904 [Primary]
GS1	20680651200901 [Package]; Contains: 10680651200904; Package: Dispenser [50 Units]; In Commercial Distribution
GS1	30680651200908 [Package]; Package: Case [4 Units]; In Commercial Distribution

FDA Product Code

• KGO: Surgeon'S Gloves

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: 2024-07-22
• Device Publish Date: 2024-07-12

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