Diametrics Medical, Ltd.
Country not established
- Devices
- 11
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Search and filter all 11 devicesFDA recalls
2003
- 14 Jul 2003 Z-1072-03 Unclassified (pre-2012) Terminated An incorrect lot designation, when entered into the blood analysis device, caused the device to give an error message and not operate.
Full distribution text
- 14 Jul 2003 Z-1072-03 Unclassified (pre-2012) Terminated An incorrect lot designation, when entered into the blood analysis device, caused the device to give an error message and not operate.
Frequently asked questions
How many devices does Diametrics Medical, Ltd. have in the registry?
The registry currently lists 11 devices for Diametrics Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diametrics Medical, Ltd.'s devices?
Among its 11 most recently registered devices, Diametrics Medical, Ltd. has devices listed in FDA 510(k) (11 devices).
What risk classes do Diametrics Medical, Ltd.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Diametrics Medical, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Diametrics Medical, Ltd.?
FDA recall records list 1 recall initiated by Diametrics Medical, Ltd., the most recent initiated on 2003-07-14. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Diametrics Medical, Ltd. in the registry?
The most recently registered devices listed for Diametrics Medical, Ltd. include IRMA BLOOD ANALYSIS SYSTEM, IRMA BLOOD ANALYSIS SYSTEM WITH OPTIONAL LIFESCAN SURESTEP PRO BLOOD GLUCOSE MODULE, TRENDCARE CALIBRATOR MODEL SCU 7007 and NEUROTREND MULTIPARAMETER SENSOR, C7004S, TO OPERATE WITH PARATREND 7+ MULTIPARAMETER SENSOR, MPM7001S, AND SATELLITE MS.