Disposable Anesthesia Circuit
- Primary DI
- 10709078004886
- Brand
- Disposable Anesthesia Circuit
- Company
- WESTMED, INC.
- Model
- 6788
- Device description
- Anesthesia Circuit, Adult, 72" Expandable, GSE w/Cap, Parallel Wye, 3L Latex Free Breathing Bag, B/V Filter, Series 700 Large Adult Mask
- Published
- 2017-10-20
- 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 |
|---|---|
| OFP | Anesthesia Breathing Circuit Kit (Adult & Pediatric) |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| OFP | Anesthesia Breathing Circuit Kit (Adult & Pediatric) | Anesthesiology | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10709078004886 | Package | GS1 | 20 | In Commercial Distribution |
| 00709078004889 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10709078004886 | 10709078004886 | ||
| 00709078004889 | 00709078004889 | 709078004889 | 0709078004889 |
GMDN Terms#
| Term | Definition |
|---|---|
| Heat/moisture exchanger/microbial filter, non-sterile | A non-sterile device intended to be placed within a breathing circuit proximal to the patient, to remove and retain microbes whilst capturing the patient's exhaled heat and moisture so that they can be used to heat and humidify the therapeutic gases inspired by the patient. It is typically a plastic housing which contains both a bidirectional microbial filter, intended to reduce the risk of cross-contamination between patients, and a heat/moisture exchanger (HME), intended to maintain the mucous membranes of the respiratory tract. It is typically used during anaesthesia or periods of prolonged respiratory support/therapy. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 092673953
- 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
- false
- 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 |
|---|---|---|---|---|
| 00709078007781 | Composite Respiratory Kit | 0799 | 2019-10-18 | |
| 00709078012693 | Septal-H Infant Size | CP-5500A | 2021-10-08 | |
| 00709078012716 | Septal-H Pediatric Size | CP-5510A | 2021-10-08 | |
| 00709078012990 | Capette | CP-4201 | 2021-06-25 | |
| 00709078013003 | Capette | CP-4202 | 2021-06-25 | |
| 00709078013010 | Capette | CP-4203 | 2021-06-25 | |
| 00709078013027 | Capette | CP-4401 | 2021-06-25 | |
| 00709078013034 | Capette | CP-4402 | 2021-06-25 | |
| 00709078013041 | Capette | CP-4403 | 2021-06-25 | |
| 00709078013058 | Strapette | CP-4204 | 2021-06-25 | |
| 00709078013065 | Strapette | CP-4220 | 2021-06-25 | |
| 00709078013072 | Strapette | CP-4404 | 2021-06-25 | |
| 00709078013089 | Strapette | CP-4420 | 2021-06-25 | |
| 00709078013096 | Chinstrap | CP-5100 | 2021-06-25 | |
| 00709078013102 | Chinstrap | CP-5200 | 2021-06-25 | |
| 00709078013119 | Septal-H | CP-5400 | 2021-06-30 | |
| 00709078013126 | Septal-H | CP-5410 | 2021-06-30 | |
| 00709078013133 | Septal-H | CP-5500 | 2021-06-30 | |
| 00709078013140 | Septal-H | CP-5510 | 2021-06-30 | |
| 00709078013157 | SavEar | RT-6100 | 2021-06-25 |
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