Intersept®
- Primary DI
- 20673978707352
- Brand
- Intersept®
- Company
- MEDTRONIC, INC.
- Model
- 1338
- Device description
- FILTER 1338 PEDIATRIC ARTERIAL 8PK 8L
- Published
- 2015-06-09
- 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 |
|---|---|
| DTM | Filter, blood, cardiopulmonary bypass, arterial line |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DTM | Filter, Blood, Cardiopulmonary Bypass, Arterial Line | Cardiovascular | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K880671 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20673978707352 | Package | GS1 | 8 | Not in Commercial Distribution |
| 00673978707358 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 20673978707352 | 20673978707352 | ||
| 00673978707358 | 00673978707358 | 673978707358 | 0673978707358 |
GMDN Terms#
| Term | Definition |
|---|---|
| Cardiopulmonary bypass system filter, arterial blood line | A sterile, porous device used in the arterial line of an extracorporeal circuit, during a cardiopulmonary bypass procedure, to trap and remove potentially harmful gaseous emboli, aggregated blood constituents, and particles greater than a specified size (e.g., 40 microns) to prevent them from flowing into the bloodstream and obstructing extracorporeal circulation. It is commonly referred to as a bubble trap and will typically be used for a specified length of time (e.g., 6 hours). This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 006261481
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- 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 |
|---|---|---|---|---|
| 00199150062911 | N/A | AFR-00213 | 2026-09-04 | |
| 00613994733658 | Pulmonary Wedge Pressure Catheter | 150075 | 2016-06-12 | |
| 00613994811639 | Z2 | Z26JR405 | 2016-06-11 | |
| 00613994813053 | Z2 | Z26EBU355 | 2016-06-11 | |
| 00643169356979 | Z2 | Z27FR40D | 2016-04-25 | |
| 00643169356993 | Z2 | Z27AL75D | 2016-06-11 | |
| 00643169559820 | Euphora™ | EUP1510X | 2016-04-25 | |
| 00643169559837 | Euphora™ | EUP1512X | 2016-04-11 | |
| 00643169559844 | Euphora™ | EUP1515X | 2016-04-11 | |
| 00643169559851 | Euphora™ | EUP1520X | 2016-04-11 | |
| 00643169559868 | Euphora™ | EUP2006X | 2016-04-11 | |
| 00643169559875 | Euphora™ | EUP2010X | 2016-04-11 | |
| 00643169559905 | Euphora™ | EUP2020X | 2016-04-11 | |
| 00643169559912 | Euphora™ | EUP2025X | 2016-04-25 | |
| 00643169559929 | Euphora™ | EUP2030X | 2016-04-11 | |
| 00643169559936 | Euphora™ | EUP22506X | 2016-04-11 | |
| 00643169559943 | Euphora™ | EUP22510X | 2016-04-11 | |
| 00643169559950 | Euphora™ | EUP22512X | 2016-04-11 | |
| 00643169559967 | Euphora™ | EUP22515X | 2016-04-11 | |
| 00643169559974 | Euphora™ | EUP22520X | 2016-04-11 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 08054117372446 | TRILLY | EUROSETS SRL | DTM | 2026-05-05 |
| 08054117372545 | HORIZON | EUROSETS SRL | DTM | 2026-05-05 |
| B00962623 | OCS HEART LEUKOCYTE DEPLETING FILTER | TRANSMEDICS, INC. | DTM | 2026-05-04 |
| 08033178112857 | Kids | SORIN GROUP ITALIA SRL | DTM | 2025-10-31 |
| 08033178112871 | Kids | SORIN GROUP ITALIA SRL | DTM | 2025-10-31 |
| 08033178114561 | MICRO | SORIN GROUP ITALIA SRL | DTM | 2025-03-04 |
| 08033178114578 | MICRO | SORIN GROUP ITALIA SRL | DTM | 2025-03-04 |
| 08033178114608 | MICRO | SORIN GROUP ITALIA SRL | DTM | 2025-03-04 |
| 38033178114562 | MICRO | SORIN GROUP ITALIA SRL | DTM | 2025-03-04 |
| 38033178114579 | MICRO | SORIN GROUP ITALIA SRL | DTM | 2025-03-04 |
| 38033178114609 | MICRO | SORIN GROUP ITALIA SRL | DTM | 2025-03-04 |
| 08033178113342 | INSPIRE | SORIN GROUP ITALIA SRL | DTM | 2021-04-13 |
| 08033178113359 | INSPIRE | SORIN GROUP ITALIA SRL | DTM | 2021-04-13 |
| 08033178113366 | INSPIRE | SORIN GROUP ITALIA SRL | DTM | 2021-04-13 |
| 38033178113343 | INSPIRE | SORIN GROUP ITALIA SRL | DTM | 2021-04-13 |
| 04037691180038 | PLEGIOX Heat Exchanger with Cardioplegia | Maquet Cardiopulmonary AG | DTM | 2017-05-02 |
| 04037691253862 | QUART | Maquet Cardiopulmonary AG | DTM | 2017-03-13 |
| 04037691173412 | QUART | Maquet Cardiopulmonary AG | DTM | 2017-03-13 |
| 04037691117911 | QUART | Maquet Cardiopulmonary AG | DTM | 2017-03-13 |
| 04037691229591 | PLEGIOX Cardioplegia Heat Exchanger | Maquet Cardiopulmonary AG | DTM | 2017-03-13 |
| 04058863017341 | QUADROX-i | Maquet Cardiopulmonary AG | DTM | 2017-02-16 |
| 04058863017372 | QUADROX-i | Maquet Cardiopulmonary AG | DTM | 2017-02-16 |
| 04058863019055 | QUADROX-i | Maquet Cardiopulmonary AG | DTM | 2017-02-16 |
| 04058863019079 | QUADROX-i | Maquet Cardiopulmonary AG | DTM | 2017-02-16 |
| 04058863019147 | QUADROX-i | Maquet Cardiopulmonary AG | DTM | 2017-02-16 |
| 04058863019185 | QUADROX-i | Maquet Cardiopulmonary AG | DTM | 2017-02-16 |
| 04058863019000 | QUADROX-iD | Maquet Cardiopulmonary AG | DTM | 2017-02-16 |
| 04058863019024 | QUADROX-iD | Maquet Cardiopulmonary AG | DTM | 2017-02-16 |
| 04058863019154 | QUADROX-i | Maquet Cardiopulmonary AG | DTM | 2017-02-16 |
| 04058863019178 | QUADROX-i | Maquet Cardiopulmonary AG | DTM | 2017-02-16 |