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Sign in to claim this brandSALTER LABS
United States·US-MF-000007934
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 30, Spur Drive, El Paso, United States
- Website
- myairlife.com
- —
- —
- [email protected]
- Phone
- +1-269-873-0502
- PRRC Contact
- Robert Yamashita
- EUDAMED SRN
- US-MF-000007934
- FDA FEI Number
- 3004748541
- DUNS Number
- 022721133
Catalogue (988)
Page 16 of 20| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Parker Flex-Tip | H-PFOL-50 | FDA UDI | Class II | Active |
| PneumoTherm | 5800-0-1 | FDA UDI | Class II | Active |
| Parker | H-PFRC-50 | FDA UDI | Class II | Active |
| Parker | H-PFRC-70 | FDA UDI | Class II | Active |
| Salter ETCo2/O2 Cannula | 4MSF1SOFT-7-13 | FDA UDI | Class II | Active |
| IntuBrite | 6015.C | FDA UDI | Class I | Active |
| Grippies | GR102C-0-110 | FDA UDI | Class I | Active |
| Parker | H-PFRC-85 | FDA UDI | Class II | Active |
| Salter ETCo2/O2 Cannula | 4MSF2SOFT-PED-7-6 | FDA UDI | Class II | Active |
| Parker | H-PFLP-90 | FDA UDI | Class II | Active |
| Parker | H-PFTDL-39 | FDA UDI | Class II | Active |
| CapnuVue | 4745-14-15 | FDA UDI | Class II | Active |
| IntuBrite | 6040.C | FDA UDI | Class I | Active |
| ThermiSense | 5750-7 | FDA UDI | Class II | Active |
| IntuBrite | 1024.C | FDA UDI | Class I | Active |
| O2 Cannula | 001321U | FDA UDI | Class I | Active |
| O2 Cannula | FM2625U | FDA UDI | Class I | Active |
| Parker Flex-Tip | H-PFUO-40 | FDA UDI | Class II | Active |
| Salter AIRE Elite | SO-1611BE | FDA UDI | Class I | Active |
| Parker Flex-Tip | H-PFNU-90 | FDA UDI | Class II | Active |
| Salter Labs | SO-2184 | FDA UDI | Class I | Active |
| Parker Flex-Tip | H-PFHV-90 | FDA UDI | Class II | Active |
| Salter AIRE Elite | SO-1777RD | FDA UDI | Class I | Active |
| Parker | H-PFST-75 | FDA UDI | Class II | Active |
| Parker Flex-Tip | H-PFNU-45 | FDA UDI | Class II | Active |
| ThermiSense | 5754-7-7 | FDA UDI | Class II | Active |
| InfuseIT | ZIT-502 | FDA UDI | Class I | Active |
| Silhouette | OTC-104-6 (QTY 1) | FDA UDI | Class I | Active |
| Parker Flex-Tip | H-PFRC-80 | FDA UDI | Class II | Active |
| Parker Flex-Tip | H-PFTVPU-65 | FDA UDI | Class II | Active |
| Parker | H-PFNU-85 | FDA UDI | Class II | Active |
| IntuBrite Sterile | S01-1021.C2016.C | FDA UDI | Class I | Active |
| Parker Flex-Tip | H-PFEC-50 | FDA UDI | Class II | Active |
| Salter AIRE Elite | 8350-8900 | FDA UDI | Class I | Active |
| IntuBrite | 2010.C | FDA UDI | Class I | Active |
| Parker | H-PSTDR-32 | FDA UDI | Class II | Active |
| Parker Flex-Tip | H-PTCY-65 | FDA UDI | Class II | Active |
| NebuTech® | 8960TG-7 | FDA UDI | Class II | Active |
| O2 Cannula | SFT2614U | FDA UDI | Class I | Active |
| O2 Cannula | 002611 | FDA UDI | Class I | Active |
| Parker Flex-Tip | H-PFHV-70 | FDA UDI | Class II | Active |
| Mindray Cannula | SO-2180 | FDA UDI | Class II | Active |
| CapnuVue | 4737-14-0 | FDA UDI | Class II | Active |
| Parker | H-PFOL-45 | FDA UDI | Class II | Active |
| IntuBrite | 6039.C | FDA UDI | Class I | Active |
| Parker | H-PFUO-55 | FDA UDI | Class II | Active |
| Parker Flex-Tip | H-PTCY-95 | FDA UDI | Class II | Active |
| Parker | H-PFUO-50 | FDA UDI | Class II | Active |
| BiNAPS | 5520-0 | FDA UDI | Class II | Active |
| Gas Sampling Lines | 0942 | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (5)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jun 25, 2014 | Z-2093-2014 | — | terminated | The case label correctly states partial rebreather but the insert label incorrectly states non-rebreather. |
| Nov 1, 2013 | Z-0360-2014 | — | terminated | It has been determined that three lots of model number 4515-15-25 CO2 Sample Line 15' tube, male Luer lock connectors may contain a 30' tube instead of the 15' length. |
| May 30, 2012 | Z-1898-2012 | — | terminated | A complaint was received, and later verified, that product labeled as SO-1296 with male luer lock connector actually contained product with a female luer lock connector. |
| Dec 7, 2011 | Z-0605-2012 | — | terminated | Mis-labeling: report of cases labeled as 4707 (cannulas with male luer lock connector) actually contained 4707F (with female luer lock connectors). |
| Oct 21, 2011 | Z-0803-2012 | — | terminated | A manufacturing defect was discovered internally which indicates that in a small number of humidifier lids, the pop-off may not occur at the appropriate pressure and can result in a leak. |