FERRIS SMITH ARTHROSCOPIC RONGEUR
- Primary DI
- 00192896035331
- Brand
- FERRIS SMITH ARTHROSCOPIC RONGEUR
- Company
- SONTEC INSTRUMENTS, INC.
- Model
- 404-812LP
- Catalog number
- 404-812LP
- Device description
- FERRIS-SMITH ARTHROSCOPIC RONGEUR DOWN SHAFT LOW PROFILE
- Published
- 2018-09-11
- 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 |
|---|---|
| HTX | RONGEUR |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| HTX | Rongeur | Orthopedic | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00192896035331 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00192896035331 | 00192896035331 | 192896035331 | 0192896035331 |
GMDN Terms
| Term | Definition |
|---|---|
| Orthopaedic joint/limb rongeur | A hand-held manual surgical instrument designed to remove bone during an orthopaedic intervention of the limbs/joints; it is not primarily intended for nasal, spinal, or cranial use and is not a dedicated rib rongeur. It is a heavy-duty metallic instrument that has a forceps- or pliers-like design and terminates at the distal end with sharp-edged, scoop-shaped jaws attached to strong, sprung (self-opening), pivoted or multi-pivoted handles that, when squeezed together, close the jaws to bite (cut) through the bone. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Length | 7 | Inch |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization;Dry Heat Sterilization |
Contacts
| Phone | |
|---|---|
| +1(800) 821-7496 | info@sontecinstruments.com |
| +1(800)821-7496 | info@sontecinstruments.com |
Regulatory Flags
- DUNS number
- 040729840
- 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
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