Curaplex® 1015-47152

GUDID 00810094577841

TritonGrip™ HV Gloves, Exam, Nitrile, Non-Sterile, Powder-Free, Textured, Orange, M

BOUND TREE MEDICAL, LLC

Nitrile examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 00810094577841
• NIH Device Record Key: 5f8e75aa-4e62-4336-8f28-7e89afc00d5a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curaplex®
• Version Model Number: 1015-47152
• Catalog Number: 1015-47152
• Company DUNS: 070556204
• Company Name: BOUND TREE MEDICAL, LLC
• Device Count: 100
• 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810094577643 [Primary]
GS1	00810094577742 [Unit of Use]
GS1	00810094577841 [Package]; Contains: 00810094577643; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• QDO: Fentanyl and other opioid protection 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: 2024-12-09
• Device Publish Date: 2024-11-30

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