A.L.P.S. mvX™ 770103010

GUDID 00196449016600

HAND SCREW RACK

Tyber Medical LLC

Instrument tray, reusable
Primary Device ID00196449016600
NIH Device Record Key509db6b8-8f17-4e7c-884b-3e76e15d764d
Commercial Distribution StatusIn Commercial Distribution
Brand NameA.L.P.S. mvX™
Version Model Number770103010
Catalog Number770103010
Company DUNS010968002
Company NameTyber Medical LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
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(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com
Phone+1(866)761-0933
Emailpreese@tybermed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100196449016600 [Primary]

FDA Product Code

FSMTRAY, SURGICAL, INSTRUMENT

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-12-25
Device Publish Date2023-12-15

On-Brand Devices [A.L.P.S. mvX™]

001964490168532.0MM FXD ANGLE/VA DBL DRL GDE
001964490168461.5MM FXD ANGLE/VA DBL DRL GDE
001964490168391.3MM FIXED ANGLE DRILL GUIDE
00196449016822T8 RETENTION DRIVER
00196449016815T6 RETENTION DRIVER
00196449016808T4 RETENTION DRIVER
001964490167921.5MM/2.0MM OFFSET PLATE 20H
001964490167851.5MM/2.0MM OFFSET PLATE 10H
00196449016778T15 RETENTION DRIVER
001964490167612.7MM OVERDRILL
00196449016754ANKLE INSTRUMENT TRAY 2
00196449016747ANKLE INSTRUMENT TRAY 1
00196449016730ANKLE OUTER CASE 1
00196449016723ANKLE OUTER CASE 2
00196449016716ANKLE SCREW RACK LID
00196449016709ANKLE SCREW RACK
00196449016693ANKLE DISTAL FIB PLT TRAY LID
00196449016686ANKLE DISTAL FIBULA PLATE TRAY
00196449016679MINI FRAG 2.0MM SCREW RACK LID
00196449016662MINI FRAG 2.0MM SCREW RACK
00196449016655MINI FRAG PLATE TRAY 1
00196449016648MINI FRAG PLATE TRAY 2
00196449016631MINI FRAG OUTER CASE
00196449016624HAND FAST GUIDE CADDY
00196449016617HAND SCREW RACK LID
00196449016600HAND SCREW RACK
00196449016594HAND PLATE TRAY
00196449016587HAND OUTER CASE
00196449016570SMALL SPIN DOWN FORCEPS
001964490165182.0MM OVERDRILL GUIDE
001964490165012.4MM OVERDRILL
001964490164952.0MM OVERDRILL
001964490164881.8MM DRILL SHORT
001964490164711.5MM DRILL SHORT
001964490164571.0MM DRILL
001964490163103.5MM NON-LOCKING SCREW 10MM
001964490163032.4MM STRAIGHT TINE PLATE 2H
00196449016297MEDIAL MALLEOLUS HOOK PLATE 5H
00196449016280MEDIAL MALLEOLUS HOOK PLATE 3H
00196449016273POSTLAT TIBIA PLATE 6-5H RT
00196449016266POSTLAT TIBIA PLATE 6-5H LT
00196449016259POSTLAT TIBIA PLATE 6-4H RT
00196449016242POSTLAT TIBIA PLATE 6-4H LT
00196449016235POSTLAT TIBIA PLATE 6-2H RT
00196449016228POSTLAT TIBIA PLATE 6-2H LT
00196449016211POSTLAT TIBIA PLATE 4-5H RT
00196449016204POSTLAT TIBIA PLATE 4-4H RT
00196449016198POSTLAT TIBIA PLATE 4-2H RT
00196449016181POSTLAT TIBIA PLATE 4-5H LT
00196449016174POSTLAT TIBIA PLATE 4-4H LT

Trademark Results [A.L.P.S. mvX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
A.L.P.S. MVX
A.L.P.S. MVX
98199222 not registered Live/Pending
Biomet C.V.
2023-09-27
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.