DR. GREENPANDA

GUDID 10850018303399

Blue Nitrile Medical Disposable Glvove

GREENPANDA SAFECARE INC.

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

• Primary Device ID: 10850018303399
• NIH Device Record Key: ed71f95c-0f31-4213-a3ce-35a537a82b27
• Commercial Distribution Discontinuation: 2030-05-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DR. GREENPANDA
• Version Model Number: MPNF12
• Company DUNS: 129509671
• Company Name: GREENPANDA SAFECARE INC.
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

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 Identifiers

Device Issuing Agency	Device ID
GS1	00850018303392 [Primary]
GS1	10850018303399 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211816

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: 2025-09-15
• Device Publish Date: 2025-09-05

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