Primary Device ID | 03613720290032 |
NIH Device Record Key | 34551bf2-9859-4b6f-9121-c3ba1ee035bc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medicrea|UNiD MIS |
Version Model Number | B33154799-01 |
Company DUNS | 383228632 |
Company Name | MEDICREA INTERNATIONAL |
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 | false |
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(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03613720290032 [Primary] |
KWQ | Appliance, fixation, spinal intervertebral body |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
[03613720290032]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-24 |
Device Publish Date | 2023-04-14 |
03613720287582 | UNiD CoCr Perc Rod 4.75mm 1-3 LV |
03613720287575 | UNiD Ti Percutaneous Rod 4.75mm 1-3 LV |
03613720287537 | UNiD CoCr Percutaneous Rod 4.75mm 4+ LV |
03613720287520 | UNiD Ti Percutaneous Rod 4.75mm 4+ LV |
03613720290254 | UNID EXP B33256099-02 CC PERC 6.0 4UPL |
03613720290230 | UNID EXP B33256099-01 CC PERC 6.0 1-3L |
03613720290216 | UNID EXP B33255599-02 CC PERC 5.5 4UPL |
03613720290193 | UNID EXP B33255599-01 CC PERC 5.5 1-3L |
03613720290179 | UNID EXP B33254799-02 CC PERC 4.75 4UPL |
03613720290155 | UNID EXP B33254799-01 CC PERC 4.75 1-3L |
03613720290131 | UNID EXP B33156099-02 TI PERC 6.0 4UPL |
03613720290117 | UNID EXP B33156099-01 TI PERC 6.0 1-3L |
03613720290094 | UNID EXP B33155599-02 TI PERC 5.5 4UPL |
03613720290070 | UNID EXP B33155599-01 TI PERC 5.5 1-3L |
03613720290056 | UNID EXP B33154799-02 TI PERC 4.75 4UPL |
03613720290032 | UNID EXP B33154799-01 TI PERC 4.75 1-3L |