Coblation
- Primary DI
- 00817470000481
- Brand
- Coblation
- Company
- Smith & Nephew, Inc.
- Model
- H0970-11
- Catalog number
- H0970-11
- Device description
- O-RING CABLE
- Published
- 2015-08-29
- 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 |
|---|---|
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | General, Plastic Surgery | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20817470000485 | Package | GS1 | 5 | In Commercial Distribution |
| 00817470000481 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 20817470000485 | 20817470000485 | ||
| 00817470000481 | 00817470000481 | 817470000481 | 0817470000481 |
GMDN Terms
| Term | Definition |
|---|---|
| Electrosurgical system generator | A mains electricity-powered (AC-powered) component of a electrosurgical system intended to generate radio-frequency (RF) electrical current for subsequent cutting and coagulation of soft tissues during an endoscopic or open surgical procedure; it is not dedicated to focal ablation of specific tissues (i.e., not a radio-frequency ablation system generator). It includes controls, may include an integrated surgical plume (smoke) suction unit, and is intended to be connected via a cable to an electrosurgical handpiece and electrode (neither of these are included); it is not intended for argon-enhanced electrosurgery. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(800)238-7538 | GUDID@SMITH-NEPHEW.COM |
Regulatory Flags
- DUNS number
- 109903521
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- 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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