CANCELLO-PURE
- Primary DI
- 00889797040532
- Brand
- CANCELLO-PURE
- Company
- WRIGHT MEDICAL TECHNOLOGY, INC.
- Model
- 4666H101
- Catalog number
- 4666H101
- Published
- 2016-09-17
- 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 |
|---|---|
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| LXH | Orthopedic Manual Surgical Instrument | Orthopedic | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00889797040532 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00889797040532 | 00889797040532 | 889797040532 | 0889797040532 |
GMDN Terms
| Term | Definition |
|---|---|
| Orthopaedic implant/instrument dismantling device | A device designed to dismantle (take apart) the component parts of an implant or a surgical instrument that have previously been assembled. It may be used as a stand-alone device or in combination with another device to control the dismantling process of, e.g., complex implants (e.g., a modular vertebral implant that has to be dismantled if the combination of the component parts do not fit the required size) or instruments so that these are correctly disassembled, without causing damage to any of the parts. It is typically made from high-grade stainless steel and/or synthetic material and is available in a variety of shapes and lengths. This is a reusable device. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(800)238-7117 | customerservice@wmt.com |
Regulatory Flags
- DUNS number
- 807201207
- 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
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00889797023443 | INVISION | 60002501 | 2016-09-17 | |
| 00889797024136 | INVISION | 60012400 | 2016-09-17 | |
| 00889797024143 | INVISION | 60012401 | 2016-09-17 | |
| 00889797040686 | NA | 49411XL | 2016-09-17 | |
| 00889797040693 | NA | 49412XL | 2016-09-17 | |
| 00889797040709 | NA | 49413XL | 2016-09-17 | |
| 00889797057295 | EZ FRAME | EF003700 | 2015-10-24 | |
| 00889797058452 | EZ FRAME SIDEKICK | EF001600 | 2016-09-17 | |
| 00889797102957 | NA | EF002550 | EF002550 | 2022-06-23 |
| 00889797103084 | NA | EF003005 | EF003005 | 2022-06-23 |
| 00889797103107 | NA | EF003700 | EF003700 | 2022-06-23 |
| 00889797023368 | INVISION | 60002201 | 2016-09-17 | |
| 00889797023375 | INVISION | 60002300 | 2016-09-17 | |
| 00889797023382 | INVISION | 60002301 | 2016-09-17 | |
| 00889797023436 | INVISION | 60002500 | 2016-09-17 | |
| 00889797023337 | INVISION | 60002100 | 2016-09-17 | |
| 00889797023344 | INVISION | 60002101 | 2016-09-17 | |
| 00889797023351 | INVISION | 60002200 | 2016-09-17 | |
| 00889797107679 | Made-To-Order | SMS00456 | SMS00456 | 2022-12-08 |
| 00889797108188 | Made-To-Order | SMS00494 | SMS00494 | 2022-12-08 |
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