Primary Device ID | 06939488383548 |
NIH Device Record Key | b67580ae-7913-468a-9910-8e04535ab753 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Milestone Spinal System |
Version Model Number | 9300005 |
Company DUNS | 545249039 |
Company Name | Shandong Weigao Orthopaedic Device Co., Ltd. |
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 | false |
Serial Number | true |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06939488383548 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-03-24 |
06939488383692 | 9300020 |
06939488383685 | 9300019 |
06939488383678 | 9300018 |
06939488383661 | 9300017 |
06939488383654 | 9300016 |
06939488383647 | 9300015 |
06939488383630 | 9300014 |
06939488383623 | 9300013 |
06939488383616 | 9300012 |
06939488383609 | 9300011 |
06939488383593 | 9300010 |
06939488383586 | 9300009 |
06939488383579 | 9300008 |
06939488383562 | 9300007 |
06939488383555 | 9300006 |
06939488383548 | 9300005 |
06939488383531 | 9300004 |
06939488383524 | 9300003 |
06939488383517 | 9300002 |
06912547325383 | 9300032 |
06912547325376 | 9300031 |
06912547325369 | 9300030 |
06912547325352 | 9300029 |
06912547325345 | 9300028 |
06912547325338 | 9300027 |
06912547325321 | 9300026 |
06912547325314 | 9300025 |
06912547325307 | 9300024 |
06912547325291 | 9300023 |
06912547325284 | 9300022 |
06912547325277 | 9300021 |