Indigo System
- Primary DI
- 00815948025455
- Brand
- Indigo System
- Company
- PENUMBRA, INC.
- Model
- LITNGBT7STR130-A
- Device description
- CAT7 130 STR plus Lightning Bolt, no CE
- Published
- 2023-02-23
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| QEW | Peripheral Mechanical Thrombectomy With Aspiration |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| QEW | Peripheral Mechanical Thrombectomy With Aspiration | Cardiovascular | 2 |
Premarket Details
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|
| K223186 | 000 | Indigo® Aspiration System Lightning Bolt Aspiration Tubing | Penumbra, Inc. | 2023-02-13 | QEW |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00815948025455 | Primary | GS1 | 0 | |
GMDN Terms
| Term | Definition |
|---|
| Thrombectomy suction catheter | A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device. |
Regulatory Flags
- DUNS number
- 191077671
- 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
- true
- Sterilization required before use
- false
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|---|
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Other Devices Sharing Product Codes
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|---|
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| 00810169722220 | Indigo System | PENUMBRA, INC. | QEW | 2026-03-10 |
| 00810169722237 | Indigo System | PENUMBRA, INC. | QEW | 2026-03-10 |
| 00810169722244 | Indigo System | PENUMBRA, INC. | QEW | 2026-03-10 |
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| M917VRG7513B30 | RoVo Mechanical Thrombectomy System | Verge Medical, Inc. | QEW | 2026-02-06 |
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| 00810123710256 | Artix AX | INARI MEDICAL INC | QEW | 2026-01-06 |
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