Migada, Ltd.
Country not established
- Devices
- 16
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What Migada, Ltd. makes
Migada, Ltd. manufactures intravenous (IV) administration systems, including high-flow IV sets, extension sets, and phthalate-free IV components. Their portfolio also covers blood gas monitoring systems for arterial blood analysis, safety cannulas for laboratory use, and specialized infusion sets for emergency and military applications. Filtration sets (1.2-micron and 3.0-micron) and multi-channel infusion devices complete the product range.
The company’s devices are classified under FDA categories Class I, Class II, and Class III, with regulatory submissions recorded in the FDA 510(k) database. These products are intended for use in the US and are subject to applicable medical device regulations. The manufacturer is based in the United States.
Catalogue
Search and filter all 16 devicesFDA recalls
FDA recall records list 1 recall initiated by Migada, Ltd., initiated on 2008-12-18. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2008
- 18 Dec 2008 Z-1244-2009 Unclassified (pre-2012) Terminated Syringe adaptor is disintegrating when attached to the end of the syringe.
Frequently asked questions
How many devices does Migada, Ltd. have in the registry?
The registry currently lists 16 devices for Migada, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Migada, Ltd.'s devices?
Among its 16 most recently registered devices, Migada, Ltd. has devices listed in FDA 510(k) (16 devices).
What risk classes do Migada, Ltd.'s devices fall under?
Among its 16 most recently registered devices, the classes recorded for Migada, Ltd.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
Are there FDA recall records for Migada, Ltd.?
FDA recall records list 1 recall initiated by Migada, Ltd., the most recent initiated on 18 Dec 2008. 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 Migada, Ltd. in the registry?
The most recently registered devices listed for Migada, Ltd. include HIGH FLOW I.V. SET, ET - EXTENSION SETS, FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER and ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG).