Primary Device ID | 00763000973476 |
NIH Device Record Key | 557cea52-f903-4e81-8813-e3d2662e6bd1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medtronic Reusable Instruments |
Version Model Number | EX5584165 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000973476 [Primary] |
HWN | INSTRUMENT, COMPRESSION |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
[00763000973476]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-09 |
Device Publish Date | 2024-11-29 |
00613994900999 | DISTRACTOR/TRIAL X1010843 6X26 |
00613994900982 | DISTRACTOR/TRIAL X1010842 6X22 |
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00613994898326 | DISTRACTOR/TRIAL X09103479 12 X 16 X 32 |
00613994898319 | DISTRACTOR/TRIAL X09103480 12 X 16 X 36 |
00613994808257 | SCREW PFF0040 40MM FACET FIXATION ANCHOR |
00613994808240 | SCREW PFF0035 35MM FACET FIXATION ANCHOR |
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00613994806246 | TRIAL 2980922 CAPSTONE 09 X 22MM |
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00613994806062 | TRIAL 2981332 CAPSTONE 13 X 32MM |
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00613994806048 | TRIAL 2981322 CAPSTONE 13 X 22MM |
00613994806031 | TRIAL 2981136 CAPSTONE 11 X 36MM |