Primary Device ID | 00763000140083 |
NIH Device Record Key | 0129f87f-5661-4f63-bb1a-97bf145f31c0 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 9564039 |
Company DUNS | 830350380 |
Company Name | MEDTRONIC SOFAMOR DANEK, INC. |
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 | true |
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 |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Length | 90 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000140083 [Primary] |
GAD | RETRACTOR |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
[00763000140083]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-04 |
Device Publish Date | 2021-09-24 |
00643169571839 - RIALTO™ SI FUSION SYSTEM | 2025-05-16 DEVICE 74200001245 THREADED 12X45 |
00763000880101 - n/a | 2025-05-16 INSERTER 7967012 CP |
00643169500365 - CD HORIZON® Growth Rod Conversion Set | 2025-05-13 CONNECTOR 811212GR 110MM TI 5.5MM ROD S |
00763000878016 - n/a | 2025-05-13 RASP 6630919 PARALLEL 10MMX15MMX12MM |
00763000878047 - n/a | 2025-05-13 RASP 6630916 PARALLEL 7MMX15MMX12MM |
00763000891367 - CD Horizon™ ModuLeX™ Spinal System | 2025-05-13 SHANK 55900608510 ILIAC 8.5X110MM |
00763000891381 - CD Horizon™ ModuLeX™ Spinal System | 2025-05-13 SHANK 55900608560 ILIAC 8.5X60MM |
00763000280468 - CENTERPIECE™ Plate Fixation System | 2025-05-12 TRAY 8530107R CENTERPIECE INSTRUMENTS |