Welch Allyn, Inc.
ELI280 12-Lead Multi-Channel Electrocardiograph - Resistive color touchscreen 10.1" display, AC or battery operation with WAM Wireless Acquisition Module (includes 1 starter pack paper -…
ELI280 12-Lead Multi-Channel Electrocardiograph – Resistive color touchscreen 10.1″ display, AC or battery operation with WAM Wireless Acquisition Module (includes 1 starter pack paper – Letter, 8.5″ x 11″); current software ; Brazil power cord; AHA 10 wire, 12-lead lead set with medi-clip ends; Adult and pediatric interpretation; Suction electrodes (6) and clamps (4); Ethernet LAN + WLAN (WPA2) + USBD; Expanded storage (up to 200 ECGs);DICOM (Bidirectional communication with third party data management system)
18manufacturers in China registered for this device type
1,734catalogue numbers in this listing
4510(k) clearances naming this product code
Who Else Makes It
Concentrated in Guangdong (10), Jiangsu (2), Beijing (1). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 77 |
| Amphenol Alden Products Company | Shenzhen | Guangdong | Contract manufacturer | 24 |
| Tianjin Choice Medical Device Co., Ltd. | Tianjin | Tianjin | Contract manufacturer | 12 |
| Yahorng Dongguan Electronic Co Ltd | Guangdong | Guangdong | Contract manufacturer | 8 |
| Omron (Dalian) Co., Ltd. (Plant 1) | Dalian | Liaoning | Contract manufacturer | 7 |
| Wuhan Strong Electronics | Wuhan | Hubei | Contract manufacturer | 6 |
| Regent Electron Suzhou Co., Ltd. | Wujiang | Jiangsu | Contract manufacturer | 5 |
| Ryder Electronics (Shenzhen) Ltd. | Shenzhen | Guangdong | Contract manufacturer | 5 |
| GE Medical Systems (China) Co., Ltd. | Wuxi | Jiangsu | Contract manufacturer | 57 |
| Edan Instruments, Inc. | Shenzhen | Guangdong | Contract manufacturer | 56 |
| Beijing Choice Electronic Technololgy Co., Ltd. | Beijing | Beijing | Repacker / relabeller | 30 |
| Shenzhen Comen Medical Instruments Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 24 |
Showing 12 of 18. All 18 manufacturers in China registered for Electrocardiograph
Record
| Listed by | Welch Allyn, Inc., United States |
|---|---|
| FDA product code | DPS |
| Device type | Electrocardiograph |
| Device class | Class 2 |
| Regulation | 21 CFR 870.2340 |
| Establishment | Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer |
| 510(k) | K072449 |
| Record published | 2019-07-22 |
| Record revised | 2025-02-03 (version 10) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Over the counter | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date, serial number |
| Packaging | Pack of 10, pack of 20 |
| Distribution end date | 2026-06-05 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 901134 | In distribution | |
| 901127 | In distribution | |
| 901129 | In distribution | |
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| 901049 | In distribution | |
| 901129 | In distribution | |
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| 901134 | In distribution | |
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| 901140 | In distribution | |
| 901129 | In distribution |
Showing 250 of 300 catalogue numbers.
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| M Series Biphasic | Zoll Medical Corporation | 93 |
| ELI 380 | Mortara Instrument, Inc. | 69 |
| Patient Cable Lead Set | Mortara Instrument, Inc. | 56 |
| ELI 250c | Mortara Instrument, Inc. | 50 |
| Lutech | Lutech Industries | 49 |
| ELI 150c | Mortara Instrument, Inc. | 47 |
| Fukuda Denshi | Fukuda Denshi Co., Ltd. | 41 |
| ELI 280 | Mortara Instrument, Inc. | 41 |
| Electrocardiograph | Edan Instruments, Inc. | 38 |
| Q-Stress | Mortara Instrument, Inc. | 25 |
| XScribe | Mortara Instrument, Inc. | 22 |
| Spacelabs Healthcare | Spacelabs Healthcare (Washington), Inc | 21 |
Showing 12 of 177. All products under Electrocardiograph
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K141582 | 2014-07-11 |
| K131573 | 2013-07-03 |
| K072449 | 2007-11-29 |
| K050074 | 2005-03-22 |
Recalls Naming This Product
17 recalls name this product by its own identifiers, the UDI on its label or the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Baxter Healthcare Corporation | 510(k) number | 2025-03-24 | Class II | Process design | There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter. | 41,739 units | |
| Baxter Healthcare Corporation | 510(k) number | 2024-10-11 | Class II | Software design | There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this coul | 2461 units | |
| Baxter Healthcare Corporation | 510(k) number | 2024-10-11 | Class II | Software design | There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this coul | 399 units | |
| Baxter Healthcare Corporation | UDI-DI | 2024-10-11 | Class II | Software design | There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this coul | 1369 units | |
| Baxter Healthcare Corporation | 510(k) number | 2024-10-11 | Class II | Software design | There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this coul | 766 units | |
| Baxter Healthcare Corporation | 510(k) number | 2024-06-03 | Class II | Employee error | During manufacturing, the step to install an Electromagnetic Interference (EMI) Absorber was omitted. The purpose of the EMI absorber is to prevent EMI leakage that might potentially affect other devices in the vicinity or the device itself | 1 unit | |
| Baxter Healthcare Corporation | 510(k) number | 2023-12-08 | Class II | Software design | Potential distortion identified in electrocardiogram (ECG) readings when the Source Consistency Filter (SCF) is enabled. | 4687 units | |
| Baxter Healthcare Corporation | 510(k) number | 2023-12-08 | Class II | Software design | Potential distortion identified in electrocardiogram (ECG) readings when the Source Consistency Filter (SCF) is enabled. | 2985 units | |
| Baxter Healthcare Corporation | 510(k) number | 2022-10-31 | Class II | Process control | One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on 26 October 2022. | 1 unit | 2025-03-06 |
| Welch Allyn Inc Mortara | 510(k) number | 2021-09-03 | Class II | Software design | The devices malfunction under specific operator workflows. | 14,630 units | |
| Welch Allyn Inc Mortara | 510(k) number | 2021-03-31 | Class II | Process control | Devices do not meet IEC 60601-2-27 requirements as labeled. | 99 units | 2024-08-16 |
| Welch Allyn Inc Mortara | 510(k) number | 2021-03-31 | Class II | Process control | Devices do not meet IEC 60601-2-27 requirements as labeled. | 27 units | 2024-08-16 |
| Welch Allyn Inc Mortara | 510(k) number | 2020-03-18 | Class II | Device Design | Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment. | 78,521 units total | 2026-02-09 |
| Welch Allyn Inc Mortara | 510(k) number | 2020-03-18 | Class II | Device Design | Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment. | 78,521 units total | 2026-02-09 |
| Welch Allyn Inc Mortara | 510(k) number | 2020-03-18 | Class II | Device Design | Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment. | 78,521 units total | 2026-02-09 |
| Welch Allyn Inc Mortara | 510(k) number | 2020-03-18 | Class II | Device Design | Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment. | 78,521 units total | 2026-02-09 |
| Mortara Instrument, Inc. | 510(k) number | 2015-05-29 | Class II | Software design | Mortara Instrument, Inc. has recently become aware of a potential safety hazard involving our ELI 380 electrocardiograph. When used in a particular workflow, acquired ECG waveforms for one patient may become associated with the patient demo | 176 | 2015-08-05 |
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.