AirLife™
AirLife DuoTherm® Heater Wire Adapter, Reusable, Single Limb
12manufacturers in China registered for this device type
27catalogue numbers in this listing
2510(k) clearances naming this product code
Who Else Makes It
Concentrated in Guangdong (7), Jiangsu (2), Fujian (1). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Flexicare Medical (Dongguan) Ltd. | Dongguan | Guangdong | Contract manufacturer | 48 |
| GaleMed (Xiamen) Co., Ltd. | Xiamen | Fujian | Contract manufacturer | 33 |
| Vincent Medical (Dong Guan) Manufacturing Co., Ltd. | Dong Guan | Guangdong | Contract manufacturer | 29 |
| Shenzhen MED-Link Electronics Tech Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 18 |
| Jianerkang Medical Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 18 |
| Sunmed AP, Ltd. | Zhuhai | Guangdong | Contract manufacturer | 18 |
| Sunmed AP, Ltd., Warehouse NO. 2 | Zhuhai | Guangdong | Contract manufacturer | 16 |
| Beijing Aeonmed Co., Ltd. | Sanhe | Hebei | Contract manufacturer | 7 |
| Betacera Inc. | Suzhou | Jiangsu | Contract manufacturer | 3 |
| Chinamed Products (China) Ltd. | Gaoyao District | Guangdong | Manufacturer | 8 |
| Ninghai Guangjie Electronic Commerce Co., Ltd. | Ningbo | Zhejiang | Manufacturer | 3 |
| Vincent Medical(Dongguan)Technology Company Limited | Dongguan | Guangdong | Contract manufacturer | 2 |
Record
| Listed by | Airlife, Inc., United States |
|---|---|
| FDA product code | BTT |
| Device type | Humidifier, Respiratory Gas, (Direct Patient Interface) |
| Device class | Class 2 |
| Regulation | 21 CFR 868.5450 |
| 510(k) | K090915 |
| Record published | 2025-02-21 |
| Record revised | 2025-09-15 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, expiry date, manufacturing date, serial number |
| Storage | Storage environment temperature -20 to 50 °C; Handling environment humidity 0 to 85 % RH; Handling environment atmospheric pressure 50 to 106 KiloPascal; Special storage condition: Keep dry |
| Packaging | Case of 10, case of 1000, box of 100, case of 14, case of 50, case of 6 |
| Distribution end date | 2025-09-12 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 377PR5E | In distribution | |
| 377CBRE | In distribution | |
| 002003 | In distribution | |
| AH290 | In distribution | |
| 377PWR90 | In distribution | |
| 377ADL | In distribution | |
| 377PWR | In distribution | |
| 5251 | In distribution | |
| 377HTR | In distribution | |
| 5257 | In distribution | |
| 2D0735X | In distribution | |
| 2D0737 | In distribution | |
| AH115-05E | In distribution | |
| 002002 | In distribution | |
| 377BR303 | In distribution | |
| 377ASL | In distribution | |
| 377PR6 | In distribution | |
| 2D0735X | In distribution | |
| 377BR201 | In distribution | |
| 377PR6E | In distribution | |
| 377BR101 | Withdrawn | |
| 377BR102 | Withdrawn | |
| 377BR301 | Withdrawn | |
| 377BR103 | Withdrawn | |
| 377BR302 | Withdrawn | |
| 377BR304 | Withdrawn | |
| 377BR305 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Hudson RCI | Teleflex Medical LLC | 160 |
| Fisher & Paykel Healthcare | Fisher & Paykel Healthcare, Ltd. | 151 |
| Vapotherm | Vapotherm Inc. | 134 |
| Humidifier, Respiratory Gas, (Direct Patient Interface) | Salter Labs | 96 |
| Hudson RCI | Medline Industries, Inc. | 41 |
| Fisher and Paykel Healthcare | Fisher & Paykel Healthcare, Ltd. | 20 |
| F&P Optiflow Junior 2 | Fisher & Paykel Healthcare, Ltd. | 17 |
| MR850 | Fisher & Paykel Healthcare, Ltd. | 13 |
| AirLife | Carefusion | 13 |
| softFlow | TNI Medical AG | 11 |
| F&P Optiflow+ | Fisher & Paykel Healthcare, Ltd. | 7 |
| AnaPod | Westmed, Inc. | 7 |
Showing 12 of 138. All products under Humidifier, Respiratory Gas, (Direct Patient Interface)
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K802852 | 1981-02-26 |
| K801252 | 1980-06-04 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.