A.L.P.S.® ELBOW SYSTEM 231218001

GUDID 00887868435737

Biomet Orthopedics, LLC

Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable Manual orthopaedic bender, reusable
Primary Device ID00887868435737
NIH Device Record Key79115890-1a07-49e4-95ef-d5675db473ac
Commercial Distribution StatusIn Commercial Distribution
Brand NameA.L.P.S.® ELBOW SYSTEM
Version Model Number2312-18-001
Catalog Number231218001
Company DUNS129278169
Company NameBiomet Orthopedics, 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 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)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868435737 [Primary]

FDA Product Code

HXPINSTRUMENT, BENDING OR CONTOURING

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


[00887868435737]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-20
Device Publish Date2020-07-10

On-Brand Devices [A.L.P.S.® ELBOW SYSTEM]

008878684357372312-18-001
008878685322211312-18-804
008878685322141312-18-803
008878685322071312-18-801
008878685321911312-18-800
008878685321841312-18-708
008878685321771312-18-707
008878685321601312-18-705
008878685321531312-18-704
008878685321081312-18-609
008878685320921312-18-607
008878685320851312-18-606
008878685320781312-18-604
008878685320091312-18-308
008878685319961312-18-305
008878685319411312-18-208
008878685319341312-18-207
008878685319271312-18-205
008878685319101312-18-204

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

Mark Image

Registration | Serial
Company
Trademark
Application Date
A.L.P.S.
A.L.P.S.
86414170 not registered Dead/Abandoned
Biomet C.V.
2014-10-03
A.L.P.S.
A.L.P.S.
86122580 4795950 Live/Registered
Biomet C.V.
2013-11-19
A.L.P.S.
A.L.P.S.
85887976 not registered Dead/Abandoned
Biomet C.V.
2013-03-27

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