LEVEL ONE SMALL BONE
- Primary DI
- 00888118052148
- Brand
- LEVEL ONE SMALL BONE
- Company
- KLS-Martin L.P.
- Model
- 26-112-13-09
- Device description
- PLATE, LINOS, STR, 1.5/2.0/2.3 MM SCREW, TI-6AL-4V
- Published
- 2016-03-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HRS | Plate, fixation, bone |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HRS | Plate, Fixation, Bone | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888118052148 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888118052148 | 00888118052148 | 888118052148 | 0888118052148 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic fixation plate, non-bioabsorbable, non-sterile | A non-sterile implantable sheet of firm material intended to be attached to fractured long bone fragments with screws to bridge and stabilize the fracture gap, and shield the site from stress as the bone heals; the material is not chemically degraded or absorbed by natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is typically used to treat traumatic or pathological orthopaedic fractures; it may also be used to temporarily augment bone following a lengthening procedure, or for arthrodesis (joint fusion). This device is intended to be sterilized prior to use. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
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
- Lot or batch
- true
- 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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