Primary Device ID | 10603295226949 |
NIH Device Record Key | 4720f0ac-822a-4857-a9d6-a0d3408b0849 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PATHWAY |
Version Model Number | 9505-01-570 |
Catalog Number | 950501570 |
Company DUNS | 896498813 |
Company Name | DEPUY INTERNATIONAL LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 | false |
OTC Over-The-Counter | false |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10603295226949 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
[10603295226949]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-05-03 |
Device Publish Date | 2018-09-24 |
10603295226499 | M.B.T. PATHWAY BUSHING EXTRACTOR |
10603295227144 | PATHWAY QUICK DRILL PIN MI |
10603295227113 | PATHWAY TIBIAL/FEMORAL RM/LL 0 DEGREE |
10603295227090 | PATHWAY TIBIAL/FEMORAL LM/RL 0 DEGREE |
10603295226956 | PATHWAY FEMORAL BOW YOKE |
10603295226949 | M.B.T. PATHWAY NON-CEMENTED KEEL PUNCH BUSHING SIZE 4-7 |
10603295226932 | M.B.T. PATHWAY NON-CEMENTED KEEL PUNCH BUSHING SIZE 2-3 |
10603295226925 | M.B.T. PATHWAY NON-CEMENTED KEEL PUNCH BUSHING SIZE 1-1.5 |
10603295226529 | M.B.T. PATHWAY KEEL PUNCH BUSHING SIZE 4-7 |
10603295226512 | M.B.T. PATHWAY KEEL PUNCH BUSHING SIZE 2-3 |
10603295226505 | M.B.T. PATHWAY KEEL PUNCH BUSHING SIZE 1-1.5 |
10603295226444 | M.B.T. PATHWAY TIBIAL TEMPLATE SIZE 4.5 |
10603295224808 | PATHWAY TIBIAL STYLUS |
10603295026969 | PATHWAY TIBIAL SCREW 21mm |
10603295026860 | PATHWAY DISASSEMBLY DRIVER |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PATHWAY 98352574 not registered Live/Pending |
Pathway Medical Inc. 2024-01-11 |
PATHWAY 97803794 not registered Live/Pending |
MILESTONE & CO., LLC 2023-02-21 |
PATHWAY 97374201 not registered Live/Pending |
Indiegogo, Inc. 2022-04-21 |
PATHWAY 97374199 not registered Live/Pending |
Indiegogo, Inc. 2022-04-21 |
PATHWAY 97348034 not registered Live/Pending |
NavAlgo SAS 2022-04-05 |
PATHWAY 97293371 not registered Live/Pending |
Fedler, Teri K 2022-03-03 |
PATHWAY 97183050 not registered Live/Pending |
ClearChoice Holdings, LLC 2021-12-21 |
PATHWAY 97114163 not registered Live/Pending |
APT PATHWAY LLC 2021-11-08 |
PATHWAY 90563451 not registered Live/Pending |
Pathway Innovations and Technologies, Inc. 2021-03-05 |
PATHWAY 90536877 not registered Live/Pending |
Pathway Vet Alliance LLC 2021-02-19 |
PATHWAY 90439523 not registered Live/Pending |
NCT Holdings, Inc 2020-12-31 |
PATHWAY 88549778 not registered Live/Pending |
Ciano-Hendricks Homes, LLC 2019-07-30 |