THINFLAP SYSTEM 91-6703-50

GUDID 00841036219468

Orthopaedic bone screw, non-bioabsorbable, non-sterile

Primary Device ID	00841036219468
NIH Device Record Key	df9a9ca2-d2b5-4cee-8c38-7a8934df4088
Commercial Distribution Status	In Commercial Distribution
Brand Name	THINFLAP SYSTEM
Version Model Number	91-6703-50
Catalog Number	91-6703-50
Company DUNS	046189866
Company Name	BIOMET MICROFIXATION, INC
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	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

Phone	+1(904)741-4400
Email	FXJAX-ORDERS@ZIMMERBIOMET.COM
Phone	+1(904)741-4400
Email	FXJAX-ORDERS@ZIMMERBIOMET.COM

Device Issuing Agency	Device ID
GS1	00841036219468 [Primary]

GXR	COVER, BURR HOLE

Steralize Prior To Use	true
Device Is Sterile	false

[00841036219468]

Moist Heat or Steam Sterilization

[00841036219468]

Moist Heat or Steam Sterilization