MemoFix® Super Elastic Nitinol Staple System
- Primary DI
- 10381780246169
- Brand
- MemoFix® Super Elastic Nitinol Staple System
- Company
- Ascension Orthopedics, Inc.
- Model
- MS-2716
- Catalog number
- MS-2716
- Device description
- Integra® MemoFix® Staple SystemThe MemoFix drill stop adapter is used for precise drilling depth.
- Published
- 2017-09-05
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
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 |
|---|---|---|---|---|
| 10381780246169 | Primary | GS1 | 0 | |
| M269MS27161 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10381780246169 | 10381780246169 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical instrument/implant depth limiter, reusable | A device designed to limit the depth of insertion of a surgical instrument (e.g., a drill bit or a reamer), a trial implant, or an implant. It may be used as a stand-alone device or it may be attached to another device to control insertion depth, typically to prevent insertion below the surgical field of interest thereby avoiding damage to tissue behind or below target structures. It is typically made of high-grade stainless steel and/or synthetic material and is available in a variety of shapes and lengths. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)654-2873 | custsvcnj@integralife.com |
Regulatory Flags#
- DUNS number
- 942377524
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 10381780240310 | Cadence™ | 10203193 | 2016-08-24 | |
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| 10381780245629 | Titan™ | IP0920055001 | IMP-0920-055-001 | 2017-09-05 |
| 10381780245636 | Titan™ | IP0920064001 | IMP-0920-064-001 | 2017-09-05 |
| 10381780245643 | Titan™ | IP0920079501 | IMP-0920-0795-01 | 2017-09-05 |
| 10381780245650 | Titan™ | IMP096006401 | IMP-0960-064-01 | 2017-09-05 |
| 10381780245667 | Titan™ | IMP096006601 | IMP-0960-066-01 | 2017-09-05 |
| 10381780245674 | Titan™ | IMP096007101 | IMP-0960-071-01 | 2017-09-05 |
| 10381780245681 | Ascension® | IMP10000D | IMP-100-00D | 2017-09-05 |
| 10381780245698 | Ascension® | IMP10000P | IMP-100-00P | 2017-09-05 |
| 10381780245704 | Integra® | IMP20000D | IMP-200-00D | 2017-09-05 |
| 10381780245711 | Integra® | IMP20000P | IMP-200-00P | 2017-09-05 |
| 10381780245728 | Integra® | IMP30000 | IMP-300-00 | 2017-09-05 |
| 10381780245735 | Integra® | IMP35000 | IMP-350-00 | 2017-09-05 |
| 10381780245759 | NuGrip® CMC Implant System | IMP44200 | IMP-442-00 | 2017-09-05 |
| 10381780245766 | First Choice® DRUJ System | IMP60000 | IMP-600-00 | 2017-09-05 |
| 10381780245780 | Movement® | IMP-890-00MT | IMP-890-00MT | 2017-09-05 |
| 10381780245797 | Movement® | IMP-890-00PP | IMP-890-00PP | 2017-09-05 |
| 10381780245803 | Integra® | IMP90001 | IMP-900-01 | 2017-09-05 |
| 10381780245988 | Integra® | MAL092008501 | MAL-0920-085-01 | 2017-08-30 |
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