LEVEL ONE THORACIC
- Primary DI
- 00888118136756
- Brand
- LEVEL ONE THORACIC
- Company
- KLS-Martin L.P.
- Model
- 99-009-11-04
- Published
- 2022-11-25
- 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
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| HXX | SCREWDRIVER |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| HXX | Screwdriver | Orthopedic | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888118136756 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888118136756 | 00888118136756 | 888118136756 | 0888118136756 |
GMDN Terms
| Term | Definition |
|---|---|
| Surgical screwdriver, reusable | A non-powered tool intended to fit into a screw head (e.g., slotted, cross/hex head) for the application of rotation to introduce/remove a screw (e.g., craniofacial bone screw, dental screw) into/from a patient in association with a surgical procedure [e.g., orthopaedic, dental, computer assisted surgery (CAS), image registration]. It may also be used to connect/disconnect a device to/from another device attached to a patient (e.g., implant component, fiducial marker). The proximal end of the device may have a handle for manual use or a profiled tang that fits into an independent chuck or power driver; it is typically made of metallic and/or polymer materials. This is a reusable device. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(904)641-7746 | KLS-UDI-Info@klsmartin.com |
Regulatory Flags
- DUNS number
- 826499238
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- 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 |
|---|---|---|---|---|
| 00888118131782 | LEVEL ONE EXTREMITY | 26-066-60-09 | 2026-05-25 | |
| 00888118131799 | LEVEL ONE EXTREMITY | 26-066-70-09 | 2026-05-25 | |
| 00888118144928 | LEVEL ONE EXTREMITY | 26-950-40-07 | 2026-05-25 | |
| 00888118145284 | PURE PECTUS | 24-070-60-09 | 2026-05-25 | |
| 00888118145291 | PURE PECTUS | 24-070-62-09 | 2026-05-25 | |
| 00888118150240 | PURE PECTUS | CTM-241-100-01 | 2026-05-25 | |
| 00888118150257 | PURE PECTUS | CTM-241-101-01 | 2026-05-25 | |
| 00888118150264 | PURE PECTUS | CTM-241-200-01 | 2026-05-25 | |
| 00888118150448 | IXOS | CTM-263-100-01 | 2026-05-25 | |
| 00888118150455 | IXOS | CTM-263-101-01 | 2026-05-25 | |
| 00888118150462 | IXOS | CTM-263-202-01 | 2026-05-25 | |
| 00888118150479 | IXOS | CTM-263-202-02 | 2026-05-25 | |
| 00888118150486 | IXOS | CTM-263-202-03 | 2026-05-25 | |
| 00888118150493 | IXOS | CTM-263-202-04 | 2026-05-25 | |
| 00888118150646 | IPS | 60-011-42-09-LP | 2026-05-25 | |
| 00888118153029 | L1 STERNAL | CTM-242-302-01 | 2026-05-25 | |
| 00888118153050 | IXOS | CTM-263-203-01 | 2026-05-25 | |
| 00888118153067 | IXOS | CTM-263-203-02 | 2026-05-25 | |
| 00888118153074 | IXOS | CTM-263-203-03 | 2026-05-25 | |
| 00888118153081 | IXOS | CTM-263-203-04 | 2026-05-25 |
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| 00190776418328 | Millennium | Avalign Technologies, Inc. | HXX | 2026-03-23 |
| 00199150039524 | n/a | MEDTRONIC SOFAMOR DANEK, INC. | HXX | 2026-03-22 |
| 00199150067459 | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | HXX | 2026-03-20 |
| B922F004800208 | ACURA Stabilization System | INDIUS MEDICAL TECHNOLOGIES PRIVATE LIMITED | HXX | 2026-03-11 |
| G832F00500340 | ACURA Stabilization System | Bioalign Inc. | HXX | 2026-03-09 |
| G832F00503040 | ACURA Stabilization System | Bioalign Inc. | HXX | 2026-03-09 |
| 00840194498975 | Response 5.5/6.0 | ORTHOPEDIATRICS CORP. | HXX | 2026-03-03 |
| 00840194498982 | Response 5.5/6.0 | ORTHOPEDIATRICS CORP. | HXX | 2026-03-03 |
| 00810076338545 | Momentum MIS - Modified Instrument | Ulrich Medical Usa, Inc. | HXX | 2026-03-02 |
| 00199150066902 | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | HXX | 2026-02-28 |
| 03662663128780 | PathFinder NXT Minimally Invasive Pedicle Screw System | Highridge Medical, LLC | HXX | 2026-02-11 |
| 03662663129084 | Lineum Occipito-Cervico-Thoracic (OCT) Spinal Fixation System | Highridge Medical, LLC | HXX | 2026-02-11 |
| 00810112597493 | TriLeap Lower Extremity Anatomic Plating System | CROSSROADS EXTREMITY SYSTEMS | HXX | 2026-02-10 |
| 00810112599756 | TriLeap Lower Extremity Anatomic Plating System | CROSSROADS EXTREMITY SYSTEMS | HXX | 2026-02-10 |
| 10886982351586 | NA | Synthes GmbH | HXX | 2026-02-10 |
| 10886982351593 | NA | Synthes GmbH | HXX | 2026-02-10 |
| 00840180545225 | General Instruments | ALPHATEC SPINE, INC. | HXX | 2026-01-29 |
| 10885862657060 | CSB | Exactech, Inc. | HXX | 2026-01-28 |
| 00840194498128 | Response Spine System | ORTHOPEDIATRICS CORP. | HXX | 2026-01-22 |
| 00888118145871 | LEVEL ONE | KLS-Martin L.P. | HXX | 2026-01-19 |
| 08800308499696 | INNOVERSE Spinal System | CG MedTech Co.,Ltd. | HXX | 2026-01-19 |
| 07640332471548 | PERLA ® TL | SpineArt SA | HXX | 2026-01-05 |
| 00840180543917 | General Instruments | ALPHATEC SPINE, INC. | HXX | 2025-12-31 |
| 00840194495189 | Response 5.5/6.0 | ORTHOPEDIATRICS CORP. | HXX | 2025-12-31 |
| 00199150060115 | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | HXX | 2025-12-29 |
| 00199150062898 | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | HXX | 2025-12-29 |
| 00888480489849 | Solitaire Cervical Spacer System | Highridge Medical, LLC | HXX | 2025-12-29 |
| 00888480489856 | Solitaire Cervical Spacer System | Highridge Medical, LLC | HXX | 2025-12-29 |