Kerrison Ronguer
- Primary DI
- 00840199520411
- Brand
- Kerrison Ronguer
- Company
- KOROS U.S.A., INC.
- Model
- 7380-81
- Catalog number
- 7380-81
- Device description
- Kerrison Ronguer 1.3mm x 40 Degree Tip, 5" Handle 9"
- Published
- 2021-11-01
- 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 |
|---|---|
| HTX | Rongeur |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HTX | Rongeur | Orthopedic | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00840199520411 | Direct Marking | GS1 | 0 | |
| 10840199520418 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00840199520411 | 00840199520411 | 840199520411 | 0840199520411 |
| 10840199520418 | 10840199520418 |
GMDN Terms#
| Term | Definition |
|---|---|
| Craniofacial rongeur, reusable | A hand-held manual surgical instrument with sharp, scoop-shaped jaws designed for cutting tough tissues (cartilage, sinew) or bone, through a cutting/biting action, during surgery involving the cranium and/or face (e.g., craniotomy, ethmoidectomy, mastoidectomy, rhinoplasty); it is not dedicated to dental surgery. It is typically made of metal and designed to withstand the forces required to bite over tough/hard tissue. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Store in dry place at room temperature |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| 1-805-529-0825 | customerservice@korosUSA.com |
Regulatory Flags#
- DUNS number
- 007928633
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- true
- 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 |
|---|---|---|---|---|
| 10840199515995 | Fiberoptic Dual End Cable | 7332-60 | 7332-60 | 2024-12-31 |
| 10840199516008 | Fiberoptic Light Port | 7332-62 | 7332-62 | 2024-12-31 |
| 10840199516015 | Fiberoptic Light Port | 7332-64 | 7332-64 | 2024-12-31 |
| 10840199531056 | Impactor | 7585-02 | 7585-02 | 2022-03-01 |
| 10840199531186 | Impactor | 7585-44 | 7585-44 | 2022-03-01 |
| 10840199528834 | Comfort Plus Chisel | 7540-06 | 7540-06 | 2025-01-31 |
| 00840199528837 | Comfort Plus Chisel | 7540-06 | 7540-06 | 2025-01-31 |
| 10840199500007 | Dilator Tube Set, Single Use, Sterile | 7332-99D | 7332-99D | 2022-01-31 |
| 10840199507723 | Separator | 7230-10 | 7230-10 | 2024-12-31 |
| 10840199507730 | Separator | 7230-15 | 7230-15 | 2024-12-31 |
| 10840199507747 | Elevator | 7230-18 | 7230-18 | 2024-12-31 |
| 10840199507754 | Elevator | 7230-20 | 7230-20 | 2024-12-31 |
| 10840199507761 | Elevator | 7230-25 | 7230-25 | 2024-12-31 |
| 10840199507778 | Elevator | 7230-30 | 7230-30 | 2024-12-31 |
| 10840199507785 | Elevator | 7230-35 | 7230-35 | 2024-12-31 |
| 10840199507792 | Elevator | 7230-40 | 7230-40 | 2024-12-31 |
| 10840199507808 | Elevator | 7230-42 | 7230-42 | 2024-12-31 |
| 10840199507815 | Elevator | 7230-43 | 7230-43 | 2024-12-31 |
| 10840199507877 | Elevator | 7230-60 | 7230-60 | 2024-12-31 |
| 10840199507907 | Hook | 7232-05 | 7232-05 | 2024-12-31 |
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| G586NS34214310 | Novo Surgical | NOVO SURGICAL, INC. | HTX | 2024-02-22 |
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