SMARTSET
- Primary DI
- 20603295168352
- Brand
- SMARTSET
- Company
- DEPUY (IRELAND)
- Model
- 3102-080
- Catalog number
- 3102080
- Device description
- SmartSet ENDURANCE MV Medium Viscosity Bone Cement 80g
- 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 |
|---|---|
| KIH | DISPENSER, CEMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KIH | Dispenser, Cement | Orthopedic | 1 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K033382 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20603295168352 | Package | GS1 | 10 | In Commercial Distribution |
| 30603295168359 | Package | GS1 | 20 | In Commercial Distribution |
| 10603295168355 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 20603295168352 | 20603295168352 |
| 30603295168359 | 30603295168359 |
| 10603295168355 | 10603295168355 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic cement, non-medicated | A substance designed to be used in arthroplastic and/or osteosynthetic procedures for the fixation of polymer or metallic implants to the living bone. It may also be intended for use as a filler in the case of bone pathologies (e.g., to stabilize and reinforce vertebral body structures in vertebroplasty and kyphoplasty). It is typically made from methylmethacrylate, polymethylmethacrylate (PMMA), esters of methacrylic acid or copolymers containing polymethylmethacrylate and polystyrene. This device does not contain an antimicrobial agent. After application, this device cannot be reused. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Handling Environment Temperature | 0 | 25 Degrees Celsius |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)255-2500 | xx@xx.xx |
Regulatory Flags#
- DUNS number
- 989365556
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- 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 |
|---|---|---|---|---|
| 10603295079941 | AML EXCEL | 2001-42-000 | 200142000 | 2018-09-24 |
| 10603295080008 | AML EXCEL | 2001-47-000 | 200147000 | 2018-09-24 |
| 10603295080015 | AML EXCEL | 2001-48-000 | 200148000 | 2018-09-24 |
| 10603295080022 | AML EXCEL | 2001-49-000 | 200149000 | 2018-09-24 |
| 10603295080145 | NA | 2001-80-501 | 200180501 | 2018-09-24 |
| 10603295080770 | NA | 2002-25-000 | 200225000 | 2018-09-24 |
| 10603295080787 | NA | 2002-27-000 | 200227000 | 2018-09-24 |
| 10603295080794 | NA | 2002-31-000 | 200231000 | 2018-09-24 |
| 10603295082057 | TRI-LOCK | 2012-03-005 | 201203005 | 2018-09-24 |
| 10603295082064 | TRI-LOCK | 2012-03-010 | 201203010 | 2018-09-24 |
| 10603295082071 | TRI-LOCK | 2012-03-020 | 201203020 | 2018-09-24 |
| 10603295082088 | TRI-LOCK | 2012-03-030 | 201203030 | 2018-09-24 |
| 10603295082095 | TRI-LOCK | 2012-03-040 | 201203040 | 2018-09-24 |
| 10603295082101 | TRI-LOCK | 2012-03-050 | 201203050 | 2018-09-24 |
| 10603295082118 | TRI-LOCK | 2012-03-060 | 201203060 | 2018-09-24 |
| 10603295082125 | TRI-LOCK | 2012-03-070 | 201203070 | 2018-09-24 |
| 10603295082132 | TRI-LOCK | 2012-03-080 | 201203080 | 2018-09-24 |
| 10603295082149 | TRI-LOCK | 2012-03-090 | 201203090 | 2018-09-24 |
| 10603295082156 | TRI-LOCK | 2012-03-100 | 201203100 | 2018-09-24 |
| 10603295082163 | TRI-LOCK | 2012-03-110 | 201203110 | 2018-09-24 |
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| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 08031497003689 | Mendec® Kypho Set Monolateral 10 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003696 | Mendec® Kypho Set Monolateral 15 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003702 | Mendec® Kypho Set Monolateral 20 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003801 | Mendec® Kypho Set Bilateral 10 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003818 | Mendec® Kypho Set Bilateral 15 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003825 | Mendec® Kypho Set Bilateral 20 mm | TECRES SPA | KIH | 2025-12-17 |
| 06923558507569 | Kyphoplasty Tool Kit | Jiangsu Changmei Medtech Co., Ltd. | KIH | 2025-10-23 |
| 06923558509693 | Kyphoplasty Tool Kit | Jiangsu Changmei Medtech Co., Ltd. | KIH | 2025-10-23 |
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| 08053617183774 | Pressurizer | ADLER ORTHO SPA | KIH | 2025-08-07 |
| 08053617183781 | Pressurizer | ADLER ORTHO SPA | KIH | 2025-08-07 |
| 08053617183798 | Pressurizer | ADLER ORTHO SPA | KIH | 2025-08-07 |
| 08053617183804 | Pressurizer | ADLER ORTHO SPA | KIH | 2025-08-07 |
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