Primary Device ID | 00822409016242 |
NIH Device Record Key | 871658f7-1033-45d8-8a17-7c748cec9d14 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tri-plus |
Version Model Number | 138-2609 |
Company DUNS | 876542390 |
Company Name | Ortho Development Corporation |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com | |
Phone | +1(801)553-9991 |
customerservice@odev.com |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Outer Diameter | 26 Millimeter |
Length | 9 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00822409016242 [Primary] |
LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-11-30 |
Device Publish Date | 2023-11-22 |
00822409016433 | 36mm -6 CoCr |
00822409016426 | 36mm -3 CoCr |
00822409016419 | 36mm +9 CoCr |
00822409016402 | 36mm +6 CoCr |
00822409016396 | 36mm +3 CoCr |
00822409016389 | 36mm +0 CoCr |
00822409016372 | 32mm -6 CoCr |
00822409016365 | 32mm -3 CoCr |
00822409016358 | 32mm +9 CoCr |
00822409016341 | 32mm +6 CoCr |
00822409016334 | 32mm +3 CoCr |
00822409016327 | 32mm +0 CoCr |
00822409016310 | 28mm -6 CoCr |
00822409016303 | 28mm -3 CoCr |
00822409016297 | 28mm +9 CoCr |
00822409016280 | 28mm +6 CoCr |
00822409016273 | 28mm +3 CoCr |
00822409016266 | 28mm +0 CoCr |
00822409016259 | 12/14 CoCr Fem Head 26mm -3 |
00822409016242 | 12/14 CoCr Fem Head 26mm +9mm |
00822409016235 | 12/14 CoCr Fem Head 26mm +6mm |
00822409016228 | 12/14 CoCr Fem Head 26mm +3mm |
00822409016211 | 12/14 CoCr Fem Head 26mm +0mm |
00822409016204 | 12/14 CoCr Fem Head 22mm -3 |
00822409016198 | 12/14 CoCr Fem Head 22mm +6 |
00822409016181 | 12/14 CoCr Fem Head 22mm +3 |
00822409016174 | 12/14 CoCr Fem Head 22mm + 0 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRI-PLUS 78594860 3294844 Live/Registered |
Ortho Development Corporation 2005-03-24 |