7250

GUDID 07613252083788

Nostril Retainer - Size 13

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	07613252083788
NIH Device Record Key	8ea913f3-9c12-4fa0-843a-150621e04365
Commercial Distribution Status	In Commercial Distribution
Version Model Number	7250
Catalog Number	7250
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

Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter
Device Size Text, specify	0
Width	29 Millimeter
Length	35 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613252083788 [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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