NA
- Primary DI
- 00889797998512
- Brand
- NA
- Company
- WRIGHT MEDICAL TECHNOLOGY, INC.
- Model
- PSCL0000
- Catalog number
- PSCL0000
- Device description
- WMT Extremity Procedure Kit
- 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
- true
- Single use
- true
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 |
|---|---|---|---|---|
| 00889797998512 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00889797998512 | 00889797998512 | 889797998512 | 0889797998512 |
GMDN Terms
| Term | Definition |
|---|---|
| General external orthopaedic fixation system implantation kit, single-use | A collection of non-sterile, manual surgical instruments intended to be used for the placement of an external orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It includes various instruments [e.g., retractors, rods, clamps, drills, pins/screws, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of external orthopaedic fixation system (i.e., non-dedicated); it does not include any implantable devices. This is a single-use device. |
Sterilization Methods
| Method |
|---|
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
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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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