ProMax™ Series Bard® Max-Blade™ Coagulating Resector
- Primary DI
- 10801741018487
- Brand
- ProMax™ Series Bard® Max-Blade™ Coagulating Resector
- Company
- C. R. Bard, Inc.
- Model
- 355214
- Catalog number
- 355214
- Device description
- ProMax™ Series Bard® Max-Blade™ Coagulating Resector, Resectoscope Compatibility: Storz Double Stem 27 Fr.
- Published
- 2016-07-23
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| FAS | ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| FAS | Electrode, Electrosurgical, Active, Urological | Gastroenterology, Urology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10801741018487 | Package | GS1 | 5 | In Commercial Distribution |
| 00801741018480 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10801741018487 | 10801741018487 | ||
| 00801741018480 | 00801741018480 | 801741018480 | 0801741018480 |
GMDN Terms
| Term | Definition |
|---|---|
| Endoscopic electrosurgical electrode, bipolar, single-use | An invasive, distal component of an electrosurgical assembly intended to deliver electrosurgical current in a bipolar configuration (i.e., without a 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 controlling ring-handles). This is a single-use device intended to be used in a sterile condition. |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(800)526-4455 | medical.services@crbard.com |
Regulatory Flags
- DUNS number
- 016898496
- 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
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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| 10801741122016 | Bard® Robinson Catheter | 0037220 | 0037220 | 2016-07-23 |
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| 10801741122108 | Bard® Robinson Catheter | 0037380 | 0037380 | 2016-07-23 |
| 10801741122115 | Bard® Robinson Catheter | 0037400 | 0037400 | 2016-07-23 |
| 10801741122122 | Bard® Robinson Catheter | 0037420 | 0037420 | 2016-07-23 |
| 10801741122139 | Bard® Robinson Catheter | 0037440 | 0037440 | 2016-07-23 |
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