Portex
- Primary DI
- 30351688410805
- Brand
- Portex
- Company
- Smiths Medical International Ltd
- Model
- 225-3710-807
- Published
- 2016-10-11
- 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
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 |
|---|---|---|---|---|
| 30351688410805 | Package | GS1 | 20 | In Commercial Distribution |
| 10351688410801 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 30351688410805 | 30351688410805 |
| 10351688410801 | 10351688410801 |
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
- true
- No natural rubber latex
- false
- 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 | |
| 30351688005896 | Portex | 563090 | 2015-07-29 | |
| 30351688018858 | Portex | 563080 | 2015-07-29 | |
| 30351688036715 | Portex | 563100 | 2015-07-29 | |
| 30351688041122 | Portex | 526060 | 2015-07-29 | |
| 30351688041139 | Portex | 526070 | 2015-07-29 | |
| 50351688041140 | Portex | 526080 | 2015-07-29 | |
| 30351688041153 | Portex | 526090 | 2015-07-29 | |
| 35019315052617 | Portex | 100/856/075 | 2015-09-01 | |
| 30351688415510 | Portex | 225-3524-804 | 2016-10-11 |
Other Devices Sharing Product Codes#
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|---|---|---|---|---|
| 00612649217604 | ADULT ULTRA FLEX® | King Systems Corporation | CAI | 2026-08-21 |
| 00612649217628 | PEDIATRIC ULTRA FLEX® | King Systems Corporation | CAI | 2026-08-21 |
| 00612649217642 | ADULT ULTRA FLEX® | King Systems Corporation | CAI | 2026-08-21 |
| 00612649217666 | ADULT ULTRA FLEX® | King Systems Corporation | CAI | 2026-08-21 |
| 00612649217680 | PEDIATRIC ULTRA FLEX® | King Systems Corporation | CAI | 2026-08-21 |
| 00612649217703 | PEDIATRIC ULTRA FLEX® | King Systems Corporation | CAI | 2026-08-21 |
| 00612649217727 | ADULT ULTRA FLEX® | King Systems Corporation | CAI | 2026-08-21 |
| 06923980116179 | N/A | GaleMed Xiamen Co., Ltd. | CAI | 2026-08-19 |
| 06923980116186 | N/A | GaleMed Xiamen Co., Ltd. | CAI | 2026-08-19 |
| 06923980116193 | N/A | GaleMed Xiamen Co., Ltd. | CAI | 2026-08-19 |
| 06923980116209 | N/A | GaleMed Xiamen Co., Ltd. | CAI | 2026-08-19 |
| 05030267170289 | 22MM SMOOTHBORE BILEVEL BREATHING SYSTEM FOR NKV-330 WITH MONIT. LINE | Intersurgical Incorporated | CAI | 2026-08-18 |
| 14896138016692 | inspired™ | VINCENT MEDICAL MANUFACTURING CO., LIMITED | CAI | 2026-08-05 |
| 04719874956547 | Create Biotech | CREATE BIOTECH CO., LTD. | CAI | 2026-07-16 |
| 04719874956554 | Create Biotech | CREATE BIOTECH CO., LTD. | CAI | 2026-07-16 |
| 10889483584705 | Vital Signs™ | AIRLIFE | CAI | 2025-03-06 |
| 10889483591666 | Vital Signs™ | AIRLIFE | CAI | 2025-02-18 |
| 10889483591925 | Vital Signs™ | AIRLIFE | CAI | 2025-02-18 |
| 10889483591987 | Vital Signs™ | AIRLIFE | CAI | 2025-02-18 |
| 10889483592113 | Vital Signs™ | AIRLIFE | CAI | 2025-02-18 |
| 10889483592496 | Vital Signs™ | AIRLIFE | CAI | 2025-02-18 |
| 10889483592656 | Vital Signs™ | AIRLIFE | CAI | 2025-02-18 |
| 10889483593448 | Vital Signs™ | AIRLIFE | CAI | 2025-02-18 |
| 10889483593561 | Vital Signs™ | AIRLIFE | CAI | 2025-02-18 |
| 10889483593660 | Vital Signs™ | AIRLIFE | CAI | 2025-02-18 |
| 10889483593752 | Vital Signs™ | AIRLIFE | CAI | 2025-02-18 |
| 10889483585627 | Vital Signs™ | AIRLIFE | CAI | 2025-02-17 |
| 10889483585801 | Vital Signs™ | AIRLIFE | CAI | 2025-02-17 |
| 10889483584699 | Vital Signs™ | AIRLIFE | CAI | 2025-02-11 |
| 10889483592175 | Vital Signs™ | AIRLIFE | CAI | 2025-02-11 |