KMEDIC
- Primary DI
- 24026704279191
- Brand
- KMEDIC
- Company
- TELEFLEX INCORPORATED
- Model
- IPN014579
- Catalog number
- KM48355
- Device description
- SCREWDRIVER SINGLE SLOT 6 3/4"
- Published
- 2018-09-15
- Public version status
- Update
- 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 |
|---|---|---|---|---|
| 04026704279197 | Direct Marking | GS1 | 0 | |
| 24026704279191 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04026704279197 | 04026704279197 | 4026704279197 |
| 24026704279191 | 24026704279191 |
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. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Length | 17.2 | Centimeter |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(919)544-8000 | CS@TELEFLEX.COM |
Regulatory Flags
- DUNS number
- 002348191
- 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
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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| 20801902219385 | ARROW | EDC-00622 | EDC-00622 | 2026-03-24 |
| 30801902219405 | ARROW | EDC-00820 | EDC-00820 | 2026-03-24 |
| 20801902219415 | ARROW | EDC-00822 | EDC-00822 | 2026-03-24 |
| 20801902219460 | ARROW | EDC-00818-M | EDC-00818-M | 2026-03-24 |
| 20801902219484 | ARROW | EDC-00622-HC | EDC-00622-HC | 2026-03-24 |
| 20801902219514 | ARROW | EDC-00822-HC | EDC-00822-HC | 2026-03-24 |
| 20801902193418 | ARROW | IPN920120 | AW-04432-N | 2026-03-23 |
| 30841156103983 | SUPERCROSS | 5302 | 5302 | 2026-03-23 |
| 20841156103993 | SUPERCROSS | 5303 | 5303 | 2026-03-23 |
| 20841156104006 | SUPERCROSS | 5304 | 5304 | 2026-03-23 |
| 20841156104013 | SUPERCROSS | 5305 | 5305 | 2026-03-23 |
| 20841156104020 | SUPERCROSS | 5306 | 5306 | 2026-03-23 |
| 20841156104037 | SUPERCROSS | 5307 | 5307 | 2026-03-23 |
| 20841156104044 | SUPERCROSS | 5308 | 5308 | 2026-03-23 |
| 30841156104058 | SUPERCROSS | 5309 | 5309 | 2026-03-23 |
| 24026704941494 | PILLING | P12797 | P12797 | 2026-03-23 |
| 24026704941500 | PILLING | P12805 | P12805 | 2026-03-23 |
| 24026704941555 | PILLING | P13063 | P13063 | 2026-03-23 |
| 24026704941562 | PILLING | P13065 | P13065 | 2026-03-23 |
| 24026704941579 | PILLING | P13081 | P13081 | 2026-03-23 |
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