NA
- Primary DI
- 20845854030643
- Brand
- NA
- Company
- Conmed Corporation
- Model
- C5012A
- Catalog number
- C5012A
- Device description
- ACROMIOPLASTY ELECTRODE (ELECTRODE ONLY), QTY 5
- Published
- 2016-09-24
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HAW | Neurological stereotaxic Instrument |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HAW | Neurological Stereotaxic Instrument | Neurology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K823424 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20845854030643 | Primary | GS1 | 0 | |
| 00845854030649 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 20845854030643 | 20845854030643 | ||
| 00845854030649 | 00845854030649 | 845854030649 | 0845854030649 |
GMDN Terms#
| Term | Definition |
|---|---|
| Endoscopic electrosurgical electrode, monopolar, single-use | A sterile, invasive, distal component of an electrosurgical assembly intended to deliver electrosurgical current in a monopolar configuration (i.e., used with a patient contact return electrode) to tissues for cutting/coagulation/ablation during endoscopic (e.g., laparoscopic, arthroscopic) surgery. It is available in a variety of forms (e.g., exchangeable electrode for electrosurgical forceps, rigid electrode, flexible endoscopic probe) which may include a lumen for suction/irrigation. It does not include a handpiece or housing and has no electrical or mechanical controls (e.g., does not include ring-handles); it is not intended for gas-enhanced electrosurgery. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)237-0169 | CUSTOMER_SERVICE@CONMED.COM |
Regulatory Flags#
- DUNS number
- 071595540
- Device count
- 5
- Lot or batch
- true
- Expiration date on label
- true
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