PCD SpinePlex
- Primary DI
- 04546540434401
- Brand
- PCD SpinePlex
- Company
- STRYKER CORPORATION
- Model
- 0505586000
- Catalog number
- 0505-586-000
- Device description
- Precision System without Needle/ Radiopaque Bone Cement
- Published
- 2015-09-24
- 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
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| LOD | BONE CEMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| LOD | Bone Cement | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 34546540434402 | Package | GS1 | 4 | In Commercial Distribution |
| 04546540434401 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 34546540434402 | 34546540434402 | |
| 04546540434401 | 04546540434401 | 4546540434401 |
GMDN Terms#
| Term | Definition |
|---|---|
| Manual orthopaedic cement mixer, reusable | A hand-operated manual device designed to mix polymethylmethacrylate (PMMA) powder with methylmethacrylate monomer in order to produce polymerizing bone cement. It typically includes a single-use inner mixing bowl where the cement is mixed, an outer housing with a handcrank and driving gears connected to a disposable mixing blade(s), and a lid. The device is intended to be connected to, or placed under, a fume extraction device to prevent fumes from polluting the working environment; it is typically operated outside of the sterile surgical field. This is a reusable device. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Storage Environment Temperature | 0 | 0 |
Contacts#
| Phone | |
|---|---|
| +1(800)253-3210 | Inst.Stryker.cs@Stryker.com |
Regulatory Flags#
- DUNS number
- 196548481
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- true
- 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
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 07613327170559 | VertaPlex HV | 0406622015 | 0406-622-015 | 2016-09-23 |
| 07613327358308 | iVAS | 808010800 | 0808-010-800 | 2019-01-11 |
| 00850024195134 | MOLLI | MS-00009 | MM1012 | 2022-06-27 |
| 04546540434371 | PCD SpinePlex | 0505582000 | 0505-582-000 | 2015-09-24 |
| 04546540434388 | PCD SpinePlex | 0505583000 | 0505-583-000 | 2015-09-24 |
| 04546540434395 | PCD SpinePlex | 0505585000 | 0505-585-000 | 2015-09-24 |
| 04546540434418 | PCD | 0505587000 | 0505-587-000 | 2015-09-24 |
| 04546540434425 | PCD | 0505589000 | 0505-589-000 | 2015-09-24 |
| 07613327639032 | Broadway System | BRW8E100D-3PK01 | BRW8E100D-3PK01 | 2025-03-12 |
| 07613327639049 | Broadway System | BRW8E105D-3PK01 | BRW8E105D-3PK01 | 2025-03-12 |
| 07613327623338 | AXS Lift | LIFT074095-01 | LIFT074095-01 | 2025-03-04 |
| 07613327623352 | AXS Lift | LIFT074105-01 | LIFT074105-01 | 2025-03-04 |
| 07613327623376 | AXS Lift | LIFT074110-01 | LIFT074110-01 | 2025-03-04 |
| 07613327623390 | AXS Lift | LIFT074115-01 | LIFT074115-01 | 2025-03-04 |
| 07613327624069 | Echo | ECHO100100-01 | ECHO100100-01 | 2025-01-24 |
| 07613327624083 | Echo | ECHO100105-01 | ECHO100105-01 | 2025-01-24 |
| 07613327624106 | Broadway 8 | BRW084132-01 | BRW084132-01 | 2025-01-24 |
| 07613327561210 | Stroke Fast Pack | AXS2PK07404601 | AXS2PK07404601 | 2023-07-14 |
| 07613327561227 | Stroke Fast Pack | AXS2PK07104601 | AXS2PK07104601 | 2023-07-14 |
| 07613327519358 | AXS VECTA 46 | INC-11814-125 | INC-11814-125 | 2021-12-17 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 03760177044326 | Signature -x Cement | TEKNIMED | LOD | 2026-01-23 |
| 03760177044333 | Signature -x Cement | TEKNIMED | LOD | 2026-01-23 |
| 03760177044340 | Signature -x Cement | TEKNIMED | LOD | 2026-01-23 |
| 04260102139411 | OSTEOPAL® | Heraeus Medical GmbH | LOD | 2025-09-26 |
| 04260102139428 | OSTEOPAL® | Heraeus Medical GmbH | LOD | 2025-09-26 |
| 03760177040090 | GENTAFIX | TEKNIMED | LOD | 2025-09-02 |
| 03760177040137 | GENTAFIX | TEKNIMED | LOD | 2025-09-02 |
| 03760177043176 | GENTAFIX | TEKNIMED | LOD | 2025-09-02 |
| 07898315500901 | Bone Cement - Normal Viscosity | Biomecânica Indústria e Comércio de Produtos Ortopédicos Ltda. | LOD | 2025-04-23 |
| 07613327545258 | AutoPlex VertaPlex | STRYKER CORPORATION | LOD | 2024-11-21 |
| 08058964729033 | Arthrex Bone Cement HV | G21 SRL | LOD | 2024-10-04 |
| 08058964729040 | Arthrex Bone Cement MV | G21 SRL | LOD | 2024-10-04 |
| 08058964728647 | Arthrex Bone Cement HV | G21 SRL | LOD | 2024-09-16 |
| 08058964728678 | BRAVO HV | G21 SRL | LOD | 2024-09-16 |
| 08058964728722 | Arthrex Bone Cement HV w/G | G21 SRL | LOD | 2024-09-16 |
| 08058964728739 | Arthrex Bone Cement MV | G21 SRL | LOD | 2024-09-16 |
| 08058964728746 | Arthrex Bone Cement MV w/G | G21 SRL | LOD | 2024-09-16 |
| 08058964729002 | BRAVO MV | G21 SRL | LOD | 2024-09-16 |
| 08058964729019 | BRAVO MV+G | G21 SRL | LOD | 2024-09-16 |
| 08058964729026 | BRAVO HV+G | G21 SRL | LOD | 2024-09-16 |
| 04260056882579 | BonOs HV | OSARTIS GmbH | LOD | 2024-05-17 |
| 04260056882623 | BonOs HV Genta | OSARTIS GmbH | LOD | 2024-04-03 |
| 03770007907752 | V-STRUT Vertebral Implant | Hyprevention Inc. | LOD | 2024-02-27 |
| 03770007907769 | V-STRUT Vertebral Implant | Hyprevention Inc. | LOD | 2024-02-27 |
| 03770007907776 | V-STRUT Vertebral Implant | Hyprevention Inc. | LOD | 2024-02-27 |
| 03770007907783 | V-STRUT Vertebral Implant | Hyprevention Inc. | LOD | 2024-02-27 |
| 03770007907790 | V-STRUT Vertebral Implant | Hyprevention Inc. | LOD | 2024-02-27 |
| 03770007907806 | V-STRUT Vertebral Implant | Hyprevention Inc. | LOD | 2024-02-27 |
| 03770007907813 | V-STRUT Vertebral Implant | Hyprevention Inc. | LOD | 2024-02-27 |
| 03770007907820 | V-STRUT Vertebral Implant | Hyprevention Inc. | LOD | 2024-02-27 |