Aliquot
- Primary DI
- 30808232001137
- Brand
- Aliquot
- Company
- Stryker Corporation
- Model
- 2110-0507
- Catalog number
- 2110-0507
- Device description
- Flexible Extensions
- Published
- 2017-12-20
- Public version status
- Update
- Distribution status
- Not 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#
Product Code Classifications#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 30808232001137 | Primary | GS1 | 0 | |
| 00808232001136 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 30808232001137 | 30808232001137 | ||
| 00808232001136 | 00808232001136 | 808232001136 | 0808232001136 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic cement preparation/delivery kit | A collection of sterile surgical instruments, tools, and materials designed to prepare and apply bone cement during an orthopaedic surgical procedure (e.g., hip replacement, arthroplasty, or vertebroplasty). It typically includes items such as forceps, a mallet, cement delivery injectors, delivery tubes, and mixing devices; it may or may not include bone cement. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Storage Environment Temperature | 0 | 0 |
Contacts#
| Phone | |
|---|---|
| +1(610)640-1775 | inst.stryker.cs@stryker.com |
Regulatory Flags#
- DUNS number
- 149183167
- Device count
- 3
- 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
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 07613327524475 | Optablate | 9700015100 | 9700-015-100 | 2022-09-23 |
| 07613327638233 | Omnicurve | 1032015000 | 1032-015-000 | 2024-09-03 |
| 00857037006075 | LATERA | LATSYS24 | LATSYS24 | 2020-01-14 |
| 00857037006037 | LATERA | LATSYS20 | LATSYS20 | 2020-01-08 |
| 07613327060058 | Precision Ideal Eyes | 0502819010 | 0502-819-010 | 2016-09-23 |
| 07613327006223 | ARIA | 48755700 | 48755700 | 2019-11-20 |
| 07613327006919 | ES2 SPINAL SYSTEM | 48280082 | 48280082 | 2019-11-20 |
| 07613327006926 | ES2 SPINAL SYSTEM | 48280083 | 48280083 | 2019-11-20 |
| 07613327006940 | ES2 SPINAL SYSTEM | 48280086 | 48280086 | 2019-11-20 |
| 07613327006957 | ES2 SPINAL SYSTEM | 48280087 | 48280087 | 2019-11-20 |
| 07613327007114 | ES2 SPINAL SYSTEM | 48280311 | 48280311 | 2019-11-25 |
| 07613327007558 | XIA 3 | 48237078 | 48237078 | 2019-11-25 |
| 07613327007565 | XIA 3 | 48237079 | 48237079 | 2019-11-25 |
| 07613327067088 | ACCULIF | 800357 | 800357 | 2016-09-24 |
| 07613327067095 | ACCULIF | 800347 | 800347 | 2016-09-24 |
| 07613327114799 | XIA 4.5 EVOLUTION | 48138140 | 48138140 | 2019-11-21 |
| 07613327114812 | XIA 4.5 EVOLUTION | 48138011R | 48138011R | 2019-11-20 |
| 07613327114843 | XIA 4.5 EVOLUTION | 48138011L | 48138011L | 2019-11-20 |
| 07613327114850 | XIA 4.5 EVOLUTION | 48138101 | 48138101 | 2019-11-21 |
| 07613327114874 | ES2 SPINAL SYSTEM | 48280178 | 48280178 | 2019-11-20 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 08033737113813 | ADRIA srl - KIT OF 2 CEMENT INJECTION CANNULAS | ADRIA SRL | OAR | 2026-08-25 |
| 00199150081073 | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | KIH | 2026-07-30 |
| 00884450587713 | StabiliT® | Merit Medical Systems, Inc. | OAR | 2026-07-30 |
| 08058964729163 | KeyFix_FILLER CANNULA FOR FENESTRATED SCREW 8-16 G | G21 SRL | OAR | 2026-05-05 |
| 03701505801211 | Dynamo | TEKNIMED | OAR | 2026-02-02 |
| 03701505801228 | Dynamo | TEKNIMED | OAR | 2026-02-02 |
| 03701505801235 | Dynamo | TEKNIMED | OAR | 2026-02-02 |
| 08031497003689 | Mendec® Kypho Set Monolateral 10 mm | TECRES SPA | OAR | 2025-12-17 |
| 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 |
| 08031497003696 | Mendec® Kypho Set Monolateral 15 mm | TECRES SPA | OAR | 2025-12-17 |
| 08031497003702 | Mendec® Kypho Set Monolateral 20 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003702 | Mendec® Kypho Set Monolateral 20 mm | TECRES SPA | OAR | 2025-12-17 |
| 08031497003801 | Mendec® Kypho Set Bilateral 10 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003801 | Mendec® Kypho Set Bilateral 10 mm | TECRES SPA | OAR | 2025-12-17 |
| 08031497003818 | Mendec® Kypho Set Bilateral 15 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003818 | Mendec® Kypho Set Bilateral 15 mm | TECRES SPA | OAR | 2025-12-17 |
| 08031497003825 | Mendec® Kypho Set Bilateral 20 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003825 | Mendec® Kypho Set Bilateral 20 mm | TECRES SPA | OAR | 2025-12-17 |
| 08053617184450 | Pressurizer | ADLER ORTHO SPA | KIH | 2025-10-07 |
| 08053617184467 | Pressurizer | ADLER ORTHO SPA | KIH | 2025-10-07 |
| 08053617184474 | Pressurizer | ADLER ORTHO SPA | KIH | 2025-10-07 |
| 08053617184481 | Pressurizer | ADLER ORTHO SPA | KIH | 2025-10-07 |
| 06951233720842 | PALAGUN® | Guangzhou Clean Medical Products Manufacturing Corp. | KIH | 2025-06-05 |
| 03701505801020 | PureKit Syringe 1.5cc MV | TEKNIMED | OAR | 2025-03-31 |
| 03701505801037 | META+ System 1.5cc MV | TEKNIMED | OAR | 2025-03-31 |
| 03701505800498 | PureKit Syringe 4cc MV | TEKNIMED | OAR | 2025-03-31 |
| 15060238201633 | HiVac™ 7 Triple Mix | SUMMIT MEDICAL LIMITED | KIH | 2025-01-10 |
| 15060238201657 | HiVac™ 7 with Femoral Cement Pressuriser | SUMMIT MEDICAL LIMITED | KIH | 2025-01-10 |
| 15060238201671 | HiVac™ Syringe | SUMMIT MEDICAL LIMITED | KIH | 2025-01-10 |