ENDOLARYNGEAL MICRO KNIFE
- Primary DI
- 00192896058675
- Brand
- ENDOLARYNGEAL MICRO KNIFE
- Company
- SONTEC INSTRUMENTS, INC.
- Model
- 1301-504
- Catalog number
- 1301-504
- Device description
- ENDOLARYNGEAL MICRO KNIFE ROUND EDGE BLADE
- Published
- 2018-09-12
- 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 |
|---|---|
| LRC | INSTRUMENT, ENT MANUAL SURGICAL |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| LRC | Instrument, Ent Manual Surgical | Ear, Nose, Throat | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00192896058675 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00192896058675 | 00192896058675 | 192896058675 | 0192896058675 |
GMDN Terms
| Term | Definition |
|---|---|
| Laryngeal knife | A hand-held manual surgical instrument designed to cut and dissect laryngeal tissue, including the vocal cords, during ear/nose/throat (ENT) surgery. It is typically a one-piece instrument made of high-grade stainless steel with a long, slender shaft with a handle at the proximal end and a sharp, single-edged, cutting blade at the distal end. The blade is normally small and available in various shapes (e.g., sickle, flap, straight) according to the procedure performed (e.g., excision of cysts, adhesions, webs). This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Length | 10 | 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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