Home Green Leaf

GUDID 00608106000711

5.0gram medical exam low derma glove

UNIWARE HOUSEWARE CORP.

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

• Primary Device ID: 00608106000711
• NIH Device Record Key: 89169e47-9512-4f3f-95a5-c7fbe646034e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Home Green Leaf
• Version Model Number: C2050S
• Company DUNS: 931896372
• Company Name: UNIWARE HOUSEWARE CORP.
• 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	00608106000704 [Primary]
GS1	00608106000711 [Package]; Contains: 00608106000704; Package: Case [10 Units]; In Commercial Distribution
GS1	00608106000735 [Unit of Use]

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: 2019-06-25
• Device Publish Date: 2019-06-17

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