HemoSphere Alta
HemoSphere Alta advanced monitor (Smart Recovery)
1manufacturer
3catalogue numbers in this listing
4510(k) clearances naming this product code
7recalls on this code
Who Else Makes It
Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 77 |
Record
| Listed by | Edwards Lifesciences Technology Sarl, United States |
|---|---|
| FDA product code | DQE |
| Device type | Catheter, Oximeter, Fiber-Optic |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1230 |
| Establishment | Contract manufacturer, Specification developer, Manufacturer |
| 510(k) | K232294 |
| Record published | 2025-03-13 |
Specifications
| MRI safety | MR Unsafe |
|---|---|
| Prescription | Prescription only |
| Label carries | manufacturing date, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| ALTASR1 | In distribution | |
| ALTACR1 | In distribution | |
| ALTAALL1 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| ICU Medical | ICU Medical, Inc | 65 |
| Vital Signs™ | AirLife Finland Oy | 12 |
| Swan-Ganz | Edwards Lifesciences Technology Sarl | 7 |
| Edwards Oximetry Central Venous Catheter | Edwards Lifesciences Technology Sarl | 6 |
| Vital Signs | Carefusion Finland 320 Oy | 6 |
| HemoSphere | Edwards Lifesciences Technology Sarl | 5 |
| Swan-Ganz True Size | Edwards Lifesciences Technology Sarl | 3 |
| Flotrac | Edwards Lifesciences Technology Sarl | 3 |
| Vigileo | Edwards Lifesciences Technology Sarl | 2 |
| ForeSight IQ | Edwards Lifesciences Technology Sarl | 1 |
| Pediasat | Edwards Lifesciences Technology Sarl | 1 |
| Presep | Edwards Lifesciences Technology Sarl | 1 |
Showing 12 of 18. All products under Catheter, Oximeter, Fiber-Optic
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K160645 | 2016-06-16 |
| K110167 | 2011-02-18 |
| K060093 | 2006-04-28 |
| K053609 | 2006-02-28 |
Recalls
7 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2021-07-09 | Class II | Process control | There is a potential for internal leaks within catheters. | 70 UNITS | 2024-01-29 |
| 2021-07-09 | Class II | Process control | There is a potential for internal leaks within catheters. | 218 UNITS | 2024-01-29 |
| 2021-07-09 | Class II | Process control | There is a potential for internal leaks within catheters. | 152 units | 2024-01-29 |
| 2021-07-09 | Class II | Process control | There is a potential for internal leaks within catheters. | 178 units | 2024-01-29 |
| 2021-07-09 | Class II | Process control | There is a potential for internal leaks within catheters. | 50 units | 2024-01-29 |
| 2021-07-09 | Class II | Process control | There is a potential for internal leaks within catheters. | 200 UNITS | 2024-01-29 |
| 2020-03-27 | Class II | Under Investigation by firm | Sterile catheter kit packaging compromised. | 597 units | 2021-04-27 |
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.