DLP®
- Primary DI
- 20643169086702
- Brand
- DLP®
- Company
- MEDTRONIC, INC.
- Model
- 12118
- Device description
- SUCTION 12118 LV VENT 18FR PVC 20PK 17L
- Published
- 2016-05-21
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| DRA | CATHETER, STEERABLE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DRA | Catheter, Steerable | Cardiovascular | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K834352 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20643169086702 | Primary | GS1 | 0 | |
| 00643169086708 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 20643169086702 | 20643169086702 | ||
| 00643169086708 | 00643169086708 | 643169086708 | 0643169086708 |
GMDN Terms#
| Term | Definition |
|---|---|
| Cardiopulmonary bypass cannula, arterial | A sterile, semi-rigid or rigid tube intended to be used during open heart surgery where it is surgically inserted for perfusion of the ascending aorta, serving as a channel for the transport of pumped, oxygenated, blood from a cardiopulmonary bypass system (heart-lung machine) tubing circuit. It is typically a moulded plastic tube with stainless steel wire reinforcement, to prevent kinking/collapse, having multiple perforations or flutes at the distal end which help diffuse and disperse incoming blood. It may be inserted using a compatible trocar. Some types may be heparin coated and include a pressure monitoring port. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Catheter Gauge | 18 | French |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 006261481
- Device count
- 20
- Lot or batch
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00199150084036 | MiniMed Flex Starter Kit | MMT-8076B | 2026-07-19 | |
| 00199150084043 | MiniMed Flex Starter Kit | MMT-8076C | 2026-07-19 | |
| 00199150084050 | MiniMed Extended Supply Kit | MMT-445B | 2026-07-19 | |
| 00199150084067 | MiniMed Extended Supply Kit | MMT-445C | 2026-07-19 | |
| 00824846004721 | NA | BB12S95R5 | 2026-07-19 | |
| 00824846004738 | NA | BB12S26R | 2026-07-19 | |
| 00824846004028 | NA | BB5722R49 | 2026-07-16 | |
| 00824846003151 | NA | BB9F19R8 | 2026-07-09 | |
| 00763000520083 | N/A | A71200 | 2021-07-23 | |
| 00643169711761 | Micra™ | MC1VR01US | 2018-01-13 | |
| 00824846003472 | NA | BB10L84R9 | 2026-07-04 | |
| 00824846003687 | NA | BB4K20R4 | 2026-07-04 | |
| 00824846003700 | NA | BB4645R21 | 2026-07-04 | |
| 00824846001669 | NA | BB12T12R4 | 2026-06-28 | |
| 00824846001843 | NA | 9S63R2 | 2026-06-28 | |
| 00824846001850 | NA | 11U35R3 | 2026-06-28 | |
| 00824846001614 | NA | BB12V43R3 | 2026-06-25 | |
| 00199150083855 | NA | BB10L80R8 | 2026-06-08 | |
| 00199150083992 | NA | BB8B99R9 | 2026-06-08 | |
| 00199150084180 | NA | 1D92R4 | 2026-06-08 |
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| 00810024670536 | AuST Steerable Sheath | CENTERPOINT SYSTEMS LLC | DRA | 2026-01-12 |
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| 00810024670550 | AuST Steerable Sheath | CENTERPOINT SYSTEMS LLC | DRA | 2026-01-12 |
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| 00810024671601 | AuST Steerable Sheath | CENTERPOINT SYSTEMS LLC | DRA | 2025-11-05 |
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| 00810024671700 | AuST Steerable Sheath | CENTERPOINT SYSTEMS LLC | DRA | 2025-11-05 |
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