Hybrid MMF AXS 56-20998E

GUDID 07613327572063

Locking screw, AXS, self-drilling

Stryker Leibinger GmbH & Co. KG

Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable

Primary Device ID	07613327572063
NIH Device Record Key	e4bec14e-4892-49d5-ba24-b796e181417a
Commercial Distribution Status	In Commercial Distribution
Brand Name	Hybrid MMF AXS
Version Model Number	56-20998E
Catalog Number	56-20998E
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	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	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0
Length	8 Millimeter
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327572063 [Primary]

FDA Product Code

DZL	SCREW, FIXATION, INTRAOSSEOUS