Perflex AcryFree 33006

GUDID 07290110500788

AcryFree Thermoplastic pellets for dentures by injection molding Shade Clear /Transparent 200gr. net jar

PERFLEX LTD

Dental appliance fabrication material, thermoplastic

• Primary Device ID: 07290110500788
• NIH Device Record Key: 6276f352-594c-46f6-905b-e98707dc2ec4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Perflex AcryFree
• Version Model Number: Clear 200gr. jar
• Catalog Number: 33006
• Company DUNS: 532176000
• Company Name: PERFLEX LTD
• 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: true
• 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

Customer Support Contacts

• Phone: +97298825473
• Email: vidal@perflexltd.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290110500788 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150454

FDA Product Code

• EBI: Resin, Denture, Relining, Repairing, Rebasing

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: 2022-11-15
• Device Publish Date: 2022-11-07

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