Galaxy Unyco 99-93509

GUDID 18054242513629

GALAXY UNYCO MINI KIT INSTRUMENTS STERILE

ORTHOFIX SRL

Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding Static magnetic bedding External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use
Primary Device ID18054242513629
NIH Device Record Keycc99673a-3d26-41aa-9cd3-153ee8a40cb0
Commercial Distribution StatusIn Commercial Distribution
Brand NameGalaxy Unyco
Version Model Number1
Catalog Number99-93509
Company DUNS438793622
Company NameORTHOFIX SRL
Device Count1
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 Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it
Phone+039456719000
Emailinfo@orthofix.it

Device Identifiers

Device Issuing AgencyDevice ID
GS118054242513629 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-03-02

On-Brand Devices [Galaxy Unyco]

18054242515180GALAXY UNYCO KIT LONG CANCELLOUS SCREWS STERILE (PACK OF 2)
18054242515173GALAXY UNYCO MINI KIT FEMUR STERILE
18054242515166GALAXY UNYCO KNEE BRIDGING BOX
18054242515159GALAXY UNYCO DIAPHYSEAL FEMUR BOX
18054242513667GALAXY UNYCO DIAPHYSEAL TIBIA BOX
18054242513650GALAXY UNYCO ANKLE - BRIDGING BOX - DELTA FRAME
18054242513643GALAXY UNYCO ANKLE BRIDGING BOX - UNILATERAL FRAME
18054242513636GALAXY UNYCO CANCELLOUS SCREW KIT STERILE
18054242513629GALAXY UNYCO MINI KIT INSTRUMENTS STERILE
18054242513612GALAXY UNYCO MINI KIT ANKLE UNILATERAL STERILE
18054242513605GALAXY UNYCO MINI KIT TIBIA STERILE
18054242512325GALAXY UNYCO DIAPHYSEAL TIBIA STERILE KIT
18054242512318POWER DRILL TORQUE LIMITER
18054242512301LIMITED TORQUE WRENCH
18054242512295THREADED WIRE (PACK OF 2)

Trademark Results [Galaxy Unyco]

Mark Image

Registration | Serial
Company
Trademark
Application Date
GALAXY UNYCO
GALAXY UNYCO
86437399 5238981 Live/Registered
Orthofix S.r.l.
2014-10-28
GALAXY UNYCO
GALAXY UNYCO
79392487 not registered Live/Pending
ORTHOFIX S.R.L.
2023-12-19
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