Model note · Holter
GE HealthCare SEER 1000 Multi-Channel Digital Holter Recorder
The SEER 1000 is a small, displayless Holter recorder that stores 2 or 3 channels of ambulatory ECG for 24 hours, 48 hours or 7 days on internal flash memory. It runs on a single AAA cell and has one button and two LEDs; patient details, hookup checks and signal preview are handled over Bluetooth from a PC or iOS app, and data is read out by USB into an analysis system such as GE MARS or CardioDay. It does no cardiac analysis itself. GETEMED in Germany builds it and GE HealthCare sells it.
The model
Maker, model and type.
- Maker
- GETEMED Medizin- und Informationstechnik AG, for exclusive distribution by GE HealthCare
- Model
- SEER 1000 Multi-Channel Digital Holter Recorder
- Device type
- Holter
- Main document
- Open the public document
Key specifications
What the public record says.
| Item | Value | Source |
|---|---|---|
| ECG channels and leads | 2 or 3 channels; 3, 5 or 7 lead-wire cable options | Source |
| Recording time | 24 hours, 48 hours or 7 days depending on recorder version | Source |
| Sampling and resolution | 256 samples/s with 12 bit resolution | Source |
| Frequency response | 0.05 to 70 Hz | Source |
| Input range, CMRR and impedance | Plus or minus 6 mV input range; CMRR above 80 dB per channel; input impedance above 10 Mohm | Source |
| Pacemaker detection | Standard, on all channels | Source |
| Power | 1 x LR03/AAA alkaline or 1 x HR03/AAA NiMH rechargeable cell (the recorder does not charge it) | Source |
| Size, weight and ingress protection | 71 x 64 x 20 mm, 53 g; IP43 | Source |
| Wireless and data transfer | Bluetooth 2.1 + EDR Class 2 (up to about 10 m in open field) for setup and preview; USB 2.0 for download | Source |
| Clock accuracy | Within 30 seconds per month; synchronised to the app when a recording is started from it | Source |
| FDA clearance | K130785, SEER 1000, product code MWJ, Class II, decided 26 July 2013; predicates SEER Light Extend (K050731) and GETEMED CardioMem CM 3000-12BT (K063042) | Source |
Recalls
Recalls.
This note lists no recalls. Check the FDA recall database for the latest record.
Safety
Safety warnings from the record.
- The technical data lists no defibrillation protection for this recorder. Source
- If exposed conductive parts of electrodes or leadwires touch other conductive parts, the isolated input no longer protects against shock. Source
- Never immerse the recorder or cables, never autoclave or steam sterilise them, and avoid ammonium chloride compounds, acetone, ketones, betadine and abrasive cleaners. Source
- Remove the battery before cleaning, and do not use any accessory until it is fully dry. Source
Sources
Where this note comes from.
- GE HealthCare SEER 1000 brochure with specifications (JB02020XX)
- FDA 510(k) K130785 summary, SEER 1000
- SEER 1000 ECG recorder and software-app usage instructions, 2067634-131 Rev E (Internet Archive copy)
- openFDA recall search, SEER 1000
Not covered: The only full manual found is an Internet Archive copy of GE document 2067634-131 Rev E that appears to be machine translated back into English, with garbled tables; facts were taken only where the meaning was clear. In the blink code table the rows for codes 1 and 2 were jumbled; code 1 is listed as the firmware CRC failure from the row order, and code 2 (internal memory or solder joint fault) was left out. Codes 3 (internal clocks) and 7 (real time clock) read clearly but are not listed separately. Check every entry against an original English GE copy before publishing. No openFDA recall and no MAUDE records were found for the SEER 1000 or its 510(k). There is no service manual, so no repair, calibration or part number content.
BMEssentia knowledge drafted from public information, reviewed by Hasan Khaled Ismail on 2026-10-24. Always follow the manufacturer's instructions for use and service manual.
Holter