NA
- Primary DI
- 34546540865053
- Brand
- NA
- Company
- STRYKER CORPORATION
- Model
- 0215089000
- Catalog number
- 0215-089-000
- Device description
- Bilateral Evacuator Tube Set
- Published
- 2018-09-24
- 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#
| Code | Name |
|---|---|
| GCY | APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GCY | Apparatus, Suction, Single Patient Use, Portable, Nonpowered | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 34546540865053 | Package | GS1 | 10 | Not in Commercial Distribution |
| 04546540865052 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 34546540865053 | 34546540865053 | |
| 04546540865052 | 04546540865052 | 4546540865052 |
GMDN Terms#
| Term | Definition |
|---|---|
| Whole-blood-recovery autotransfusion system, powered | An assembly of devices used to collect, filter, and reinfuse intraoperative and/or postoperative autologous blood shed during and/or after elective and non-elective surgery. It is a complete, closed-circuit system that typically includes a suction set or a catheter for blood access, a collection unit, an autotransfusion bag, safety clamps, non-return valves, various blood screening filters, and a transfusion set. The suction mechanism is typically actuated by a central vacuum system. A trocar may also be included. The device is typically used when there is a lack of donor blood or when compatible blood is not available. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)253-3210 | Inst.Stryker.cs@Stryker.com |
Regulatory Flags#
- DUNS number
- 196548481
- Device count
- 1
- 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
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 07613252254430 | VertaPlex | 0406622000 | 0406-622-000 | 2016-09-23 |
| 04546540434364 | SpinePlex | 0406202000 | 0406-202-000 | 2016-06-30 |
| 07613154599097 | NA | 5920000201 | 5920-000-201 | 2016-09-23 |
| 07613154599103 | NA | 5920000202 | 5920-000-202 | 2018-09-24 |
| 07613154599110 | NA | 5920000203 | 5920-000-203 | 2018-09-24 |
| 07613154599134 | NA | 5920000205 | 5920-000-205 | 2018-09-24 |
| 07613154599141 | NA | 5920000206 | 5920-000-206 | 2018-09-24 |
| 07613154599158 | NA | 5920000207 | 5920-000-207 | 2018-09-24 |
| 07613154599165 | NA | 5920000208 | 5920-000-208 | 2018-09-24 |
| 07613154599172 | NA | 5920000209 | 5920-000-209 | 2018-09-24 |
| 07613154599189 | NA | 5920000301 | 5920-000-301 | 2018-09-24 |
| 07613154599196 | NA | 5920000302 | 5920-000-302 | 2018-09-24 |
| 07613154599202 | NA | 5920000303 | 5920-000-303 | 2018-09-24 |
| 07613154599219 | NA | 5920000304 | 5920-000-304 | 2018-09-24 |
| 07613154599226 | NA | 5920000305 | 5920-000-305 | 2018-09-24 |
| 07613154599233 | NA | 5920000306 | 5920-000-306 | 2018-09-24 |
| 07613154599240 | NA | 5920000307 | 5920-000-307 | 2018-09-24 |
| 07613154615513 | NA | 5920000309 | 5920-000-309 | 2018-09-24 |
| 07613327141771 | SpinePlex | 0406222000 | 0406222000 | 2016-09-23 |
| 07613327141788 | SpinePlex | 0406202010 | 0406-202-010 | 2016-09-23 |
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