0431578405

GUDID H98004315784050

1.5MM TI RAISED HEAD SCREW SELF-DRILLING/PLUSDRIVE®/4MM

SYNTHES (U.S.A.) LP

Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile 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 IDH98004315784050
NIH Device Record Keyba701cf0-b593-4fb5-8988-8235eed1864f
Commercial Distribution StatusIn Commercial Distribution
Version Model Number04.315.784.05
Catalog Number0431578405
Company DUNS832637081
Company NameSYNTHES (U.S.A.) LP
Device Count5
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS120887587072026 [Primary]
GS180887587072028 [Unit of Use]
HIBCCH98004315784050 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQNEXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


[H98004315784050]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-12-20
Device Publish Date2019-12-12

Devices Manufactured by SYNTHES (U.S.A.) LP

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H679022221160 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/16MM
H679022221180 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/18MM
H679022221200 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/20MM
H679022221220 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/22MM
H679022221240 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/24MM
H679022221260 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/26MM

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