Pure Grip 1032504

GUDID 10304040005054

Pure Grip Medium

HENRY SCHEIN, INC.

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

• Primary Device ID: 10304040005054
• NIH Device Record Key: 271731f1-5041-4d9f-9cb9-0f44a3dc006d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pure Grip
• Version Model Number: 1032504
• Catalog Number: 1032504
• Company DUNS: 012430880
• Company Name: HENRY SCHEIN, INC.
• Device Count: 100
• DM Exempt: true
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *FALSE

Device Identifiers

Device Issuing Agency	Device ID
GS1	00304040005057 [Primary]
GS1	10304040005054 [Package]; Contains: 00304040005057; Package: [20 Units]; In Commercial Distribution
GS1	20304040005051 [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: 2019-05-16
• Device Publish Date: 2019-05-08

On-Brand Devices [Pure Grip]

• 10304040005078: Pure Grip X-Large
• 10304040005061: Pure Grip Large
• 10304040005054: Pure Grip Medium
• 10304040005047: Pure Grip Small
• 10304040002602: Pure Grip X-Small
• H65810325632: Pure Grip Large
• H65810325452: Pure Grip X-Large
• H65810325232: Pure Grip X-Small
• H65810325072: Pure Grip Small
• H65810325042: Pure Grip Medium