SUBFIX XBR001001

GUDID 07613252264545

Guidewire

Stryker Trauma SA

Instrument tray

Primary Device ID	07613252264545
NIH Device Record Key	fdff6b85-081f-4334-b8f2-5e2f51d259fd
Commercial Distribution Status	In Commercial Distribution
Brand Name	SUBFIX
Version Model Number	XBR001001
Catalog Number	XBR001001
Company DUNS	481999654
Company Name	Stryker Trauma SA
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	false
Expiration Date	false
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

Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0
Length	305 Millimeter
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613252264545 [Primary]

FDA Product Code

LXH	ORTHOPEDIC MANUAL SURGICAL INSTRUMENT