Primary Device ID | 00846832072552 |
NIH Device Record Key | f2184ae0-673c-4a30-945e-f5447e2d260b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LATITUDE EV™ |
Version Model Number | 9039002 |
Company DUNS | 968990812 |
Company Name | TORNIER, 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 | 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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com | |
Phone | +1(888)494-7950 |
customerservice@tornier.com |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Outer Diameter | 6 Millimeter |
Length | 45 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00846832072552 [Primary] |
JDC | PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-16 |
Device Publish Date | 2019-05-08 |
00846832073986 | 9030356 |
00846832073979 | 9030351 |
00846832073962 | 9030346 |
00846832073955 | 9030341 |
00846832072965 | 9030398 |
00846832072941 | 9030397 |
00846832072927 | 9030395 |
00846832072590 | 9039005 |
00846832072576 | 9039004 |
00846832072569 | 9039003 |
00846832072552 | 9039002 |
00846832072545 | 9039001 |
00846832072538 | 9039000 |
00846832072521 | 0830825 |
00846832072514 | 0830824 |
00846832072507 | 0830823 |
00846832072491 | 0830822 |
00846832072484 | 0830821 |
00846832072477 | 0830820 |
00846832072460 | 0830819 |
00846832072453 | 0830818 |
00846832072446 | 0830817 |
00846832072439 | 0830816 |
00846832074815 | 0030721 |
00846832074808 | 0030720 |
00846832074754 | 0030711 |
00846832074747 | 0030710 |
00846832074693 | 0030701 |
00846832074686 | 0030700 |