7238

GUDID 07613252083665

Nostril Retainer - Size 1

Stryker Leibinger GmbH & Co. KG

Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable Intranasal splint, non-biodegradable 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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