Curaplex® 1015-47151

GUDID 00810094577834

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

BOUND TREE MEDICAL, LLC

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

• Primary Device ID: 00810094577834
• NIH Device Record Key: ccec9974-9750-4102-99a3-7799c6c9e64b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curaplex®
• Version Model Number: 1015-47151
• Catalog Number: 1015-47151
• 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	00810094577636 [Primary]
GS1	00810094577735 [Unit of Use]
GS1	00810094577834 [Package]; Contains: 00810094577636; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• LZA: Polymer 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: 2024-12-09
• Device Publish Date: 2024-11-30

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