Duragel,Pin Liner, Tapered, 3mm, Medium

GUDID 00614464182167

Silipos Holding LLC

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• Primary Device ID: 00614464182167
• NIH Device Record Key: 91735184-6a9c-4a9f-9abb-1d51f65cd64c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Duragel,Pin Liner, Tapered, 3mm, Medium
• Version Model Number: 18216
• Company DUNS: 056112948
• Company Name: Silipos Holding LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00614464182167 [Primary]

FDA Product Code

• IQO: Device, Prosthesis Alignment

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: 2022-08-15
• Device Publish Date: 2022-08-05

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