TRIALTIS
- Primary DI
- 10705034647852
- Brand
- TRIALTIS
- Company
- Medos International Sàrl
- Model
- 5161-00-5083
- Catalog number
- 5161005083
- Device description
- TRIALTIS Spine System Probe, Lumbar Straight, Navigation 0-6cm ± 4%
- Published
- 2026-07-04
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| OLO | Orthopedic stereotaxic instrument |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| OLO | Orthopedic Stereotaxic Instrument | Neurology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K233255 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10705034647852 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10705034647852 | 10705034647852 |
GMDN Terms#
| Term | Definition |
|---|---|
| Abdominal/ENT/orthopaedic surgical probe, reusable | A slender, rod-like, hand-held manual surgical instrument intended to be used to explore cavities, wounds or fistulas during abdominal, ENT, and/or orthopaedic surgical interventions; it does not include stereotactic devices and is not dedicated to endoscopy. It may have a blunt bulbous, paddle-like, or pointed tip, may be single- or double-ended, and the shaft may be straight, bent or hooked. It is made of rigid or flexible metallic and/or synthetic polymer material. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)255-2500 | xx@xx.xx |
Regulatory Flags#
- DUNS number
- 482661753
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10705034369761 | SKYLINE | 410270112 | 410270112 | 2016-12-31 |
| 10705034369778 | SKYLINE | 410270116 | 410270116 | 2016-12-31 |
| 10705034369785 | SKYLINE | 410270120 | 410270120 | 2016-12-31 |
| 10705034369822 | SKYLINE | 410270228 | 410270228 | 2016-12-31 |
| 10705034369839 | SKYLINE | 410270232 | 410270232 | 2016-12-31 |
| 10705034369846 | SKYLINE | 410270236 | 410270236 | 2016-12-31 |
| 10705034369884 | SKYLINE | 410270342 | 410270342 | 2016-12-31 |
| 10705034369891 | SKYLINE | 410270348 | 410270348 | 2016-12-31 |
| 10705034369907 | SKYLINE | 410270354 | 410270354 | 2016-12-31 |
| 10705034369983 | SKYLINE | 410290130 | 410290130 | 2016-12-31 |
| 10705034648194 | VELYS | 451611065 | 451611065 | 2026-10-09 |
| 10705034648200 | VELYS | 451611064 | 451611064 | 2026-10-09 |
| 00856879006519 | FIBERGRAFT Aeridyan | 59000170 | 59000170 | 2026-09-29 |
| 00856879006908 | FIBERGRAFT Aeridyan Matrix | 73000030 | 73000030 | 2023-04-05 |
| 00856879006915 | FIBERGRAFT Aeridyan Matrix | 73000063 | 73000063 | 2023-04-05 |
| 00856879006922 | FIBERGRAFT Aeridyan Matrix | 73000125 | 73000125 | 2023-04-05 |
| 00856879006946 | FIBERGRAFT Aeridyan Matrix | 73000200 | 73000200 | 2023-04-05 |
| 00856879006250 | FIBERGRAFT Aeridyan Matrix | 59000125 | 59000125 | 2021-08-04 |
| 00856879006281 | FIBERGRAFT Aeridyan Matrix | 59000063 | 59000063 | 2021-08-04 |
| 00856879006298 | FIBERGRAFT Aeridyan Matrix | 59000015 | 59000015 | 2021-08-04 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00190376632919 | Invictus | ALPHATEC SPINE, INC. | OLO | 2026-10-20 |
| 04056481147969 | Spine and Trauma Navigation | Brainlab SE | OLO | 2026-10-19 |
| 00889024673403 | NavitrackER® | Orthosoft Inc | OLO | 2026-06-26 |
| 00889024699762 | ROSA® Shoulder | Orthosoft Inc | OLO | 2026-06-26 |
| 00889024699779 | ROSA® Shoulder | Orthosoft Inc | OLO | 2026-06-26 |
| 00889024699786 | ROSA® Shoulder | Orthosoft Inc | OLO | 2026-06-26 |
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| 00889024674790 | ROSA PIN STABILIZER 60MM | Orthosoft Inc | OLO | 2025-12-12 |
| 00889024674776 | ROSA POLYAXIAL REFERENCE SIZE 3 | Orthosoft Inc | OLO | 2025-12-11 |
| 00889024674783 | ROSA POLYAXIAL REFERENCE SIZE 6 | Orthosoft Inc | OLO | 2025-12-11 |
| 00889024674806 | ROSA STABILIZER TISSUE DEFLECTOR 60MM | Orthosoft Inc | OLO | 2025-12-11 |
| 00889024687455 | ROSA® Knee | Orthosoft Inc | OLO | 2025-11-21 |
| 07613252286578 | FLUOROMAP | Stryker Leibinger GmbH & Co. KG | OLO | 2025-01-28 |
| 00887868557873 | ROSA® Shoulder | Orthosoft Inc | OLO | 2024-03-06 |
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| 00887868558306 | ROSA® Shoulder | Orthosoft Inc | OLO | 2024-03-06 |
| 00887868575105 | ROSA® Shoulder | Orthosoft Inc | OLO | 2024-03-06 |
| 00887868575112 | ROSA® Shoulder | Orthosoft Inc | OLO | 2024-03-06 |