Portex
- Primary DI
- 35019315088562
- Brand
- Portex
- Company
- Smiths Medical International Ltd
- Model
- C45091673D-NL
- Published
- 2017-01-03
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Related Records
Product Codes
| Code | Name |
|---|---|
| CAI | Circuit, breathing (w connector, adaptor, y piece) |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| CAI | Circuit, Breathing (W Connector, Adaptor, Y Piece) | Anesthesiology | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 35019315088562 | Package | GS1 | 20 | In Commercial Distribution |
| 15019315088568 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 35019315088562 | 35019315088562 |
| 15019315088568 | 15019315088568 |
GMDN Terms
| Term | Definition |
|---|---|
| Anaesthesia breathing circuit, single-use | An assembly of devices designed to conduct medical gases from the fresh gas supply outlet of an anaesthesia unit/workstation to the patient, typically connecting the patient, a ventilator/ventilation bag, carbon dioxide (CO2) absorber, and a monitor. It typically includes both an inhalation and exhalation route and consists of breathing tubes, a ventilation and/or reservoir bag(s), a Y-piece, connectors/adaptors, and gas sampling ports. The absorber, a one-way directional valve, and adjustable pressure limiting (APL) valve are also devices typically employed in the circuit but may not be a part of this device. This is a single-use device. |
Sterilization Methods
| Method |
|---|
Regulatory Flags
- DUNS number
- 215591523
- 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
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 30351688423256 | Portex | 008430M | 2015-09-01 | |
| 30351688423270 | Portex | 008430T | 2015-09-01 | |
| 30351688423287 | Portex | 008431T | 2015-09-01 | |
| 30351688424277 | Portex | 008435 | 2015-09-01 | |
| 30351688404002 | Portex | 002000 | 2016-10-05 | |
| 35019517223334 | Portex | C45101816D-NL | 2020-06-12 | |
| 35019517236679 | Portex | C45101817D-NL | 2020-09-18 | |
| 30351688403036 | Portex | 007767 | 2016-10-05 | |
| 30351688410249 | Portex | 002220 | 2016-12-28 | |
| 30351688410355 | Portex | 007760 | 2016-10-05 | |
| 30351688416128 | Portex | 002223 | 2016-12-28 | |
| 10351688003782 | Portex | 512070 | 2015-07-29 | |
| 30351688005896 | Portex | 563090 | 2015-07-29 | |
| 10351688017949 | Portex | 512090 | 2015-07-29 | |
| 10351688018670 | Portex | 512060 | 2015-07-29 | |
| 10351688018809 | Portex | 512100 | 2015-07-29 | |
| 30351688018858 | Portex | 563080 | 2015-07-29 | |
| 10351688036674 | Portex | 512080 | 2015-07-29 | |
| 30351688036715 | Portex | 563100 | 2015-07-29 | |
| 10351688037176 | Portex | 502060 | 2015-07-29 |
Other Devices Sharing Product Codes
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 44710810083325 | N/A | GALEMED CORPORATION | CAI | 2026-03-05 |
| 44710810085558 | N/A | GALEMED CORPORATION | CAI | 2026-03-05 |
| 44710810087682 | N/A | GALEMED CORPORATION | CAI | 2026-03-05 |
| 44710810088559 | N/A | GALEMED CORPORATION | CAI | 2026-03-05 |
| 44710810101319 | N/A | GALEMED CORPORATION | CAI | 2026-03-05 |
| 44710810103504 | N/A | GALEMED CORPORATION | CAI | 2026-03-05 |
| 44710810105720 | N/A | GALEMED CORPORATION | CAI | 2026-03-05 |
| 44710810105737 | N/A | GALEMED CORPORATION | CAI | 2026-03-05 |
| 44710810110915 | N/A | GALEMED CORPORATION | CAI | 2026-03-05 |
| 44710810116108 | N/A | GALEMED CORPORATION | CAI | 2026-03-05 |
| 44710810080867 | N/A | GALEMED CORPORATION | CAI | 2026-03-04 |
| 44710810087859 | N/A | GALEMED CORPORATION | CAI | 2026-03-04 |
| 44710810088474 | N/A | GALEMED CORPORATION | CAI | 2026-03-04 |
| 44710810089808 | N/A | GALEMED CORPORATION | CAI | 2026-03-04 |
| 44710810103146 | N/A | GALEMED CORPORATION | CAI | 2026-03-04 |
| 44710810114098 | N/A | GALEMED CORPORATION | CAI | 2026-03-04 |
| 44710810116092 | N/A | GALEMED CORPORATION | CAI | 2026-03-04 |
| 44710810116924 | N/A | GALEMED CORPORATION | CAI | 2026-03-04 |
| 20889483300135 | Respan® | SUNMED, LLC | CAI | 2026-02-11 |
| 46923980110359 | N/A | GaleMed Xiamen Co., Ltd. | CAI | 2026-02-05 |
| M368H0678972 | HAUSTED | GF HEALTH PRODUCTS, INC. | CAI | 2025-10-31 |
| 00612649214559 | UNIVERSAL F® FLEX2® | King Systems Corporation | CAI | 2023-01-18 |
| 00612649130972 | JACKSON REES | King Systems Corporation | CAI | 2023-01-18 |
| 00612649214047 | UNIVERSAL F® FLEX2® | King Systems Corporation | CAI | 2023-01-18 |
| 00612649214030 | UNIVERSAL F® FLEX2® | King Systems Corporation | CAI | 2023-01-18 |
| 00612649214078 | UNIVERSAL F® FLEX2® | King Systems Corporation | CAI | 2023-01-18 |
| 00612649214092 | UNIVERSAL F® FLEX2® | King Systems Corporation | CAI | 2023-01-18 |
| 00612649214115 | UNIVERSAL F® FLEX2® | King Systems Corporation | CAI | 2023-01-18 |
| 00612649214139 | UNIVERSAL F® FLEX2® | King Systems Corporation | CAI | 2023-01-18 |
| 00612649214153 | UNIVERSAL F® FLEX2® | King Systems Corporation | CAI | 2023-01-18 |