| Primary Device ID | H981046060220 |
| NIH Device Record Key | a7fc9246-15db-413e-af4a-8a4f6a7238ef |
| Commercial Distribution Discontinuation | 2021-09-30 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Click'X |
| Version Model Number | 04.606.022 |
| Catalog Number | 04606022 |
| Company DUNS | 832637081 |
| Company Name | SYNTHES (U.S.A.) LP |
| 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)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 | 10705034735115 [Primary] |
| HIBCC | H981046060220 [Secondary] |
| MNI | ORTHOSIS, SPINAL PEDICLE FIXATION |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
[H981046060220]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-07-12 |
| Device Publish Date | 2015-09-14 |