Soft Air
Blanket, Full Underbody, Full Access, Reflective
8manufacturers in China registered for this device type
56catalogue numbers in this listing
2510(k) clearances naming this product code
Who Else Makes It
Concentrated in Jiangsu (3), Shanghai (1), Anhui (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Sino Protection (Hefei) Medical Products Co., Ltd. | Hefei | Anhui | Contract manufacturer | 18 |
| Jiangyin Sinbon Electronics Co Ltd | Jiangyin | Jiangsu | Contract manufacturer | 13 |
| Copious Intl., Inc. | Heyuan, Guangdong Province | Contract manufacturer | 11 | |
| Jiangyin Puremed | Jiangyin | Jiangsu | Contract manufacturer | 7 |
| Betacera Inc. | Suzhou | Jiangsu | Contract manufacturer | 3 |
| Shanghai Xodus Medical Company Limited | Shanghai | Shanghai | Specification developer | 25 |
| Hangzhou Tappa Medical Technology Co., Ltd. | Hangzhou | Zhejiang | Manufacturer | 3 |
| Jiangmen Dacheng Medical Equipment Co., Ltd. | Jiangmen | Guangdong | Contract manufacturer | 1 |
Record
| Listed by | Adroit Medical Systems, Inc., United States |
|---|---|
| FDA product code | DWJ |
| Device type | System, Thermal Regulating |
| Device class | Class 2 |
| Regulation | 21 CFR 870.5900 |
| Establishment | Contract manufacturer, Manufacturer |
| 510(k) | K073712 |
| Record published | 2017-03-15 |
| Record revised | 2026-05-07 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Ethylene Oxide |
| 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 |
| Packaging | Carton of 10, carton of 5, pack of 10, pack of 40 |
| Distribution end date | 2026-05-05 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| OR110 | In distribution | |
| A250R | In distribution | |
| A220R | In distribution | |
| A260 | In distribution | |
| A510 | In distribution | |
| A250 | In distribution | |
| A290 | In distribution | |
| A400R | In distribution | |
| A220 | In distribution | |
| A240R | In distribution | |
| A240 | In distribution | |
| A260R | In distribution | |
| A550 | Withdrawn | |
| A315 | Withdrawn | |
| A560 | Withdrawn | |
| A310R | Withdrawn | |
| OR018 | Withdrawn | |
| A285 | Withdrawn | |
| A265 | Withdrawn | |
| A280 | Withdrawn | |
| A555 | Withdrawn | |
| A265R | Withdrawn | |
| OR010 | Withdrawn | |
| A542 | Withdrawn | |
| A570R | Withdrawn | |
| OR012 | Withdrawn | |
| A300R | Withdrawn | |
| A542R | Withdrawn | |
| A635R | Withdrawn | |
| OR011 | Withdrawn | |
| A230 | Withdrawn | |
| A570 | Withdrawn | |
| A1100 | Withdrawn | |
| A545 | Withdrawn | |
| A540R | Withdrawn | |
| A522R | Withdrawn | |
| A400 | Withdrawn | |
| A450R | Withdrawn | |
| A310 | Withdrawn | |
| A525 | Withdrawn | |
| A286 | Withdrawn | |
| A530 | Withdrawn | |
| A540 | Withdrawn | |
| A545R | Withdrawn | |
| A522 | Withdrawn | |
| A555R | Withdrawn | |
| A610 | Withdrawn | |
| A525R | Withdrawn | |
| A315R | Withdrawn | |
| A550R | Withdrawn | |
| A270 | Withdrawn | |
| OR014 | Withdrawn | |
| A645 | Withdrawn | |
| A300 | Withdrawn | |
| A635 | Withdrawn | |
| A230R | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Mistral-Air | The Surgical Company International B.V. | 114 |
| Bair Hugger™ | 3M Company | 99 |
| IOB | Jiangmen Dacheng Medical Equipment Co., Ltd. | 68 |
| IOB | Iob Medical, Inc. | 61 |
| 3M™ Bair Hugger™ | 3M Company | 61 |
| Cocoon | Care Essentials PTY Ltd | 59 |
| Level 1 | ICU Medical, Inc | 49 |
| System, Thermal Regulating | Hangzhou Tappa Medical Technology Co., Ltd. | 47 |
| PremierPro | Prestige Ameritech | 39 |
| Bair Paws™ | 3M Company | 30 |
| SourceMark | Sourcemark, LLC. | 25 |
| Kozee | Sourcemark, LLC. | 24 |
Showing 12 of 166. All products under System, Thermal Regulating
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K073712 | 2008-06-06 |
| K921920 | 1992-12-11 |
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.