Primary Device ID | 00819251026468 |
NIH Device Record Key | 793bf3e7-d3dc-4921-9eaf-b51f4e681614 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PS-Post Box Trial, Klassic ONE |
Version Model Number | 2165.05.000 |
Company DUNS | 078416717 |
Company Name | TOTAL JOINT ORTHOPEDICS, INC. |
Device Count | 1 |
DM Exempt | false |
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)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com | |
Phone | +1(801)486-6070 |
udi@tjoinc.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00819251026468 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
[00819251026468]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-19 |
Device Publish Date | 2020-10-09 |
00819251026482 | PS-Post Box Trial, Size 7 |
00819251026475 | PS-Post Box Trial, Size 6 |
00819251026468 | PS-Post Box Trial, Size 5 |
00819251026451 | PS-Post Box Trial, Size 4 |
00819251026444 | PS-Post Box Trial, Size 3 |
00819251026437 | PS-Post Box Trial, Size 2 |
00819251026420 | PS-Post Box Trial, Size 1 |
00819251029384 | PS-Post Box Trial, Size 7 |
00819251029377 | PS-Post Box Trial, Size 6 |
00819251029360 | PS-Post Box Trial, Size 5 |
00819251029353 | PS-Post Box Trial, Size 4 |
00819251029346 | PS-Post Box Trial, Size 3 |
00819251029339 | PS-Post Box Trial, Size 2 |
00819251029322 | PS-Post Box Trial, Size 1 |