REFLEX HYBRID
- Primary DI
- 07613327270761
- Brand
- REFLEX HYBRID
- Company
- Stryker Corporation
- Model
- 48510420
- Catalog number
- 48510420
- Device description
- TEMPORARY FIXATION PIN, LONG
- Published
- 2019-11-08
- 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
- true
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 |
|---|---|---|---|---|
| 07613327270761 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07613327270761 | 07613327270761 | 7613327270761 |
GMDN Terms#
| Term | Definition |
|---|---|
| Intraoperative orthopaedic bone pin/screw, reusable | A small rod intended to be inserted into bone to temporarily anchor a surgical instrument (e.g., retractor, implant aligner) and/or implantable device (e.g., fixation plate) to the bone during an orthopaedic surgical procedure; it is not left in situ after the procedure. It may be wholly- or partially-threaded for screwing into bone, and may have other physical features to enable fixation of surgical instruments/devices. It is made of metallic (e.g., stainless steel) or polymer (radiolucent) material and is available in various shapes and sizes. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags#
- DUNS number
- 149183167
- Device count
- 1
- DM exempt
- true
- 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#
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|---|---|---|---|---|
| 07613327665031 | Sonopet iQ+ | 550026B010 | 5500-26B-010 | 2026-10-12 |
| 07613327665048 | Sonopet iQ+ | 550026B020 | 5500-26B-020 | 2026-10-12 |
| 07613327665055 | Sonopet iQ+ | 550026B114 | 5500-26B-114 | 2026-10-12 |
| 07613327665062 | Sonopet iQ+ | 550026B312 | 5500-26B-312 | 2026-10-12 |
| 07613327687149 | Sonopet iQ+ | 550026B328 | 5500-26B-328 | 2026-10-12 |
| 07613327662030 | ALPHAVENT | 3911-856-547 | 3911-856-547 | 2025-06-16 |
| 07613327662047 | ALPHAVENT | 3911-856-555 | 3911-856-555 | 2025-06-16 |
| 07613327662054 | ALPHAVENT | 3911-856-565 | 3911-856-565 | 2025-06-16 |
| 04546540434364 | SpinePlex | 0406202000 | 0406-202-000 | 2016-06-30 |
| 07613252254430 | VertaPlex | 0406622000 | 0406-622-000 | 2016-09-23 |
| 07613327141788 | SpinePlex | 0406202010 | 0406-202-010 | 2016-09-23 |
| 07613154757091 | VertaPlex | 0406402000 | 0406-402-000 | 2016-06-30 |
| 07613327141764 | VertaPlex | 0406402002 | 0406-402-002 | 2016-09-23 |
| 07613327170559 | VertaPlex HV | 0406622015 | 0406-622-015 | 2016-09-23 |
| 07613327170566 | VertaPlex | 0406402015 | 0406-402-015 | 2016-09-23 |
| 00808232000214 | NA | 2102-0131 | 2102-0131 | 2015-09-24 |
| 07613327124200 | Vitoss VBA Pack | 2102-2401 | 2102-2401 | 2015-12-09 |
| 07613327124217 | Vitoss VBA Pack | 2101-2405 | 2102-2405 | 2015-12-09 |
| 07613327124224 | Vitoss VBA Pack | 2102-2402 | 2102-2402 | 2015-12-09 |
| 07613327124231 | Vitoss VBA Pack | 2102-2410 | 2102-2410 | 2015-12-09 |
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| 00850080243176 | OSTEOROD Delivery System | BONE SOLUTIONS, INC. | LXH | 2026-10-12 |
| 00889795150264 | APEX 3D Total Ankle Replacement System | Paragon 28, Inc. | LXH | 2026-10-12 |
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