7238

GUDID 07613252083665

Nostril Retainer - Size 1

Stryker Leibinger GmbH & Co. KG

Intranasal splint, non-biodegradable

• Primary Device ID: 07613252083665
• NIH Device Record Key: 3166134c-4191-4ceb-aa79-f35082279ba3
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 7238
• Catalog Number: 7238
• Company DUNS: 316153956
• Company Name: Stryker Leibinger GmbH & Co. KG
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter
• Width: 16 Millimeter
• Device Size Text, specify: 0
• Length: 23 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613252083665 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K981374

FDA Product Code

• LYA: SPLINT, INTRANASAL SEPTAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-24

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