Plasti-Products

GUDID 40797876141545

sharps container, red 5.4qt

PLASTI-PRODUCTS INC

Sharps container

• Primary Device ID: 40797876141545
• NIH Device Record Key: be31b2f1-926c-472d-aab0-bcd4e86717bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Plasti-Products
• Version Model Number: 143154
• Company DUNS: 153880372
• Company Name: PLASTI-PRODUCTS INC
• Device Count: 1
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com
• Phone: 1-800-527-5396
• Email: kandyo@plastiproducts.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10797876141544 [Primary]
GS1	20797876141541 [Package]; Contains: 10797876141544; Package: box [10 Units]; In Commercial Distribution
GS1	40797876141545 [Package]; Contains: 20797876141541; Package: case [2 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K970383

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-08-18
• Device Publish Date: 2016-04-15

On-Brand Devices [Plasti-Products]

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• 20797876146089: sharps container, red vertical entry,8qt - Wide Mouth
• 20797876145143: sharps container, red horizontal entry,14qt
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• 40797876143549: sharps container, yellow 5.4qt
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• 40797876142023: sharps container, clear, 5qt
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• 10797876141025: sharps container, red 5qt
• 10797876104341: sharps container, red vertical entry,14qt
• 10797876102859: sharps container, red vertical entry,8qt
• 40797876102362: sharps container, red vertical entry,4qt