KMEDIC
- Primary DI
- 24026704282016
- Brand
- KMEDIC
- Company
- TELEFLEX INCORPORATED
- Model
- IPN014823
- Catalog number
- KM49574
- Device description
- SCOVILLE CURETTE 10" STRAIGHT
- 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 |
|---|---|
| FZS | CURETTE, SURGICAL, GENERAL USE |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| FZS | Curette, Surgical, General Use | General, Plastic Surgery | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04026704282012 | Direct Marking | GS1 | 0 | |
| 24026704282016 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04026704282012 | 04026704282012 | 4026704282012 |
| 24026704282016 | 24026704282016 |
GMDN Terms
| Term | Definition |
|---|---|
| Bone curette, reusable | A manual surgical instrument designed for cutting and excising bone tissue typically during an orthopaedic or a plastic surgery procedure. It is typically designed as a long, slender instrument with a handle at the proximal end and a concave, spoon-like tip which has a sharp edge, at the distal end, or it may be double-ended, and is used to facilitate the removal of the bone tissue without causing trauma to the surrounding muscles. It is typically made of high-grade stainless steel and is a common instrument of choice for the removal of the bone. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Length | 25.4 | 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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