| Primary Device ID | 10886705029228 |
| NIH Device Record Key | 48ee34eb-d41f-47db-bd80-7112e61cc774 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 242361 |
| Catalog Number | 242361 |
| Company DUNS | 482661753 |
| Company Name | Medos International Sàrl |
| Device Count | 1 |
| DM Exempt | true |
| 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)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| Phone | +1(800)255-2500 |
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| 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 | 10886705029228 [Primary] |
| FST | LIGHT, SURGICAL, FIBEROPTIC |
| FSX | Light, surgical, connector |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-02-17 |
| Device Publish Date | 2022-02-09 |
| 10705034467214 - EXPEDIUM VERSE | 2026-03-25 EXPEDIUM VERSE SPINE SYSTEM HEAD ADJUSTER |
| 10705034005294 - KANEDA SR | 2026-03-24 KANEDA SR ANTERIOR SYSTEM INSTRUMENT HANDLE (MODULAR) |
| 10705034195148 - VIPER | 2026-03-24 VIPER F2 FACET FIXATION SYSTEM 1ST DILATOR |
| 10705034209555 - CONFIDENCE SPINAL CEMENT SYSTEM | 2026-03-24 CONFIDENCE SPINAL CEMENT SYSTEM CONFIDENCE KIT SPINAL CEMENT SYSTEM 5cc |
| 10705034209623 - CONFIDENCE SPINAL CEMENT SYSTEM | 2026-03-24 CONFIDENCE SPINAL CEMENT SYSTEM CONFIDENCE PLUS KIT SPINAL CEMENT SYSTEM 11cc |
| 10705034209630 - CONFIDENCE SPINAL CEMENT SYSTEM | 2026-03-24 CONFIDENCE SPINAL CEMENT SYSTEM CONFIDENCE KIT SPINAL CEMENT SYSTEM |
| 10705034369624 - PULSE | 2026-03-24 PULSE ANTERIOR CERVICAL PLATE SYSTEM SCREW STARTER |
| 10705034369648 - PULSE | 2026-03-24 PULSE ANTERIOR CERVICAL PLATE SYSTEM TEMPORARY FIXATION PIN |