Lifemotion
- Primary DI
- 06974762681101
- Brand
- Lifemotion
- Company
- Lifemotion Medical Technology Co., Ltd.
- Model
- LMF-10-001
- Device description
- Lifemotion Cart
- Published
- 2026-06-02
- Public version status
- New
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes#
| Code | Name |
|---|---|
| KRI | Accessory Equipment, Cardiopulmonary Bypass |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KRI | Accessory Equipment, Cardiopulmonary Bypass | Cardiovascular | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 06974762681101 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 06974762681101 | 06974762681101 | 6974762681101 |
GMDN Terms#
| Term | Definition |
|---|---|
| Cardiopulmonary bypass system centrifugal pump drive unit | A mains electricity (AC-powered) device that powers and controls the speed of a disposable cardiovascular bypass system centrifugal pump, to which it is connected, for the circulation of blood through the extracorporeal circuit for gas exchange and reinfusion. This device drives the centrifugal rotor of the disposable centrifugal pump using magnetism. |
Regulatory Flags#
- DUNS number
- 698655611
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- true
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- true
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 06974762681019 | Lifemotion | LM-BGEA-1000 | LM-BGEA-1000 | 2026-06-02 |
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