Primary Device ID | 10705034507361 |
NIH Device Record Key | 8f5993e7-8826-46de-87d9-774c9f3a5fcf |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 163005515 |
Catalog Number | 163005515 |
Company DUNS | 482661753 |
Company Name | Medos International Sàrl |
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 | true |
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)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10705034507361 [Primary] |
HRX | ARTHROSCOPE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-10-12 |
Device Publish Date | 2016-10-13 |
10705034595542 - TRIALTIS | 2024-08-26 TRIALTIS Spine System Set Screw 4 Pack T27 5.5 and 6.0 |
10705034595887 - TRIALTIS | 2024-08-26 TRIALTIS Spine System Set Screw 8 Pack T27 5.5 and 6.0 |
10705034596891 - TRIALTIS | 2024-08-26 TRIALTIS Spine System Set Screw 2 Pack T27 5.5 and 6.0 |
10705034596907 - TRIALTIS | 2024-08-26 TRIALTIS Spine System Set Screw 6 Pack T27 5.5 and 6.0 |
10705034199504 - VIPER | 2024-08-20 VIPER SYSTEM CANNULA PLUNGER |
10705034062358 - MONARCH | 2024-07-29 MONARCH SPINE SYSTEM S/C WITH WASHER, STRAIGHT 5.5mm |
10705034062365 - MONARCH | 2024-07-29 MONARCH SPINE SYSTEM S/C WITH WASHER, EXT 5.5mm |
10705034062372 - MONARCH | 2024-07-29 MONARCH SPINE SYSTEM SLOTTED CONNECTOR WITH WASHER, OFFSET, RIGHT 5.5mm |