EV1000
EV1000 Databox Assembly
5manufacturers in China registered for this device type
11catalogue numbers in this listing
11510(k) clearances naming this product code
3recalls on this code
Who Else Makes It
Concentrated in Guangdong (4), Jiangsu (1). 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 |
| Shenzhen Mindray BIO-Medical Electronics Co., Ltd. | Shenzhen | Guangdong | Specification developer | 61 |
| GE Medical Systems (China) Co., Ltd. | Wuxi | Jiangsu | Contract manufacturer | 57 |
| Orantech Inc. | Shenzhen | Guangdong | Contract manufacturer | 40 |
| Shenzhen Comen Medical Instruments Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 24 |
Record
| Listed by | Edwards Lifesciences Technology Sarl, United States |
|---|---|
| FDA product code | DXG |
| Device type | Computer, Diagnostic, Pre-Programmed, Single-Function |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1435 |
| Establishment | Contract manufacturer, Specification developer, Manufacturer |
| 510(k) | K131892 |
| Record published | 2016-09-03 |
| Record revised | 2021-11-10 (version 8) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date, serial number |
| Storage | Special storage condition: STORE IN A COOL, DRY PLACE. |
| Sizes | Length 6 to 15 ft; length 93 to 192 in |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| EV1000DB | Height: 145 mm, Width: 206 mm, Depth: 64 mm, Weight: 0.9 kg (2.0 lbs) | In distribution |
| EVPSA110L | Voltage: 110V | In distribution |
| EVFTCL | Length 15 ft | In distribution |
| EVPSB110L | Length 15 ft | In distribution |
| EVPSB110 | Voltage: 110V | In distribution |
| EVVVTC1 | Length 93 in | In distribution |
| EV1000A | MONITOR: HEIGHT: 226 MM, WIDTH: 296 MM, DEPTH: 58.6 MM, WEIGHT: 2.1 KG (4.6 LBS), DATABOX: HEIGHT: 145 MM, WIDTH: 206 MM, DEPTH: 64 MM, WEIGHT: 0.9 KG (2.0 LBS) | In distribution |
| EVEC1 | Length 6 ft | In distribution |
| EVPSA110 | Voltage: 110V | In distribution |
| EVFTC1 | Length 192 in | In distribution |
| EVECL | Length 15 ft | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| LiDCO Ltd | Lidco Ltd. | 133 |
| LiDCO | Lidco Ltd. | 32 |
| Transonic | Transonic Systems, Inc. | 31 |
| Computer, Diagnostic, Pre-Programmed, Single-Function | Edwards Lifesciences Technology Sarl | 23 |
| Retia Medical | Retia Medical, LLC | 17 |
| Computer, Diagnostic, Pre-Programmed, Single-Function | GE Healthcare Finland OY | 5 |
| Pediasat | Edwards Lifesciences Technology Sarl | 4 |
| LiDCO | Masimo Corporation | 4 |
| ICU Medical | ICU Medical, Inc | 4 |
| Cnap® Monitor 500 HD | Cnsystems Medizintechnik GmbH | 4 |
| Vigileo | Edwards Lifesciences Technology Sarl | 3 |
| Starling | Cheetah Medical (Israel) Ltd | 3 |
Showing 12 of 39. All products under Computer, Diagnostic, Pre-Programmed, Single-Function
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K193179 | 2019-12-17 |
| K131892 | 2014-05-22 |
| K131588 | 2014-05-22 |
| K110597 | 2011-06-14 |
| K103094 | 2011-05-17 |
| K100709 | 2010-12-07 |
| K082308 | 2008-12-09 |
| K062134 | 2006-08-22 |
| K060660 | 2006-04-25 |
| K043103 | 2004-12-09 |
| K040287 | 2004-04-26 |
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Edwards Lifesciences Technology Sarl | 510(k) number | 2019-03-21 | Class I | Use error | Potential for an electrical short circuit leading to possible fire hazard due to liquid ingress into AC power outlets. | 22443 | 2023-11-28 |
Recalls
The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2010-06-25 | Not classified | Process design | The recall was initiated because the Edwards’ MHANM8 Pressure Slave Cable was wired incorrectly, thus will not work as stated. | 20 units | 2011-05-24 |
| 2008-09-12 | Not classified | Device Design | Edwards Lifesciences has made the decision to initiate a field corrective action for the Edwards Vigilance II Model: Software: versions 00.51, 00.60, 00.61, 00.62, 00.63, 00.64, 00.67, 00.69, 00.71, 00.73 due to the potential of inaccurate | 6934 instruments | 2012-02-08 |
| 2007-05-17 | Not classified | Software design | MAP offset errors: If users are “slaving” mean arterial pressure (MAP) from the bedside monitor into the Vigilance II Monitor for the purpose of the continuous calculation of systemic vascular resistance (SVR), at times, on some bedside mo | 2,680 units in North America distribution | 2009-10-09 |
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.