Medimop Medical Projects, Ltd.
Country not established
- Devices
- 14
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What Medimop Medical Projects, Ltd. makes
Medimop Medical Projects, Ltd. manufactures vial connectors, transfer devices, and adapters for medical use, including products such as vial connectors with closed collars, mixing and dispensing pins with detachable vial holders and pre-attached needles, spray head attachments, swabable vial adapters in 13mm and 20mm sizes, vial-to-bag transfer systems, and vented or needleless transfer devices for 13mm vials.
The devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 14 devicesFDA recalls
FDA recall records list 1 recall initiated by Medimop Medical Projects, Ltd., initiated on 2017-10-06. By recorded status: 1 terminated. The reasons filed fall into these groups: mechanical integrity and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 1
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2017
- 6 Oct 2017 Z-0972-2018 Class II Terminated Medimop is recalling certain lots of this product Vial2Bag DC due to the potential of the IV Port separating from the Via12Bag DC body during the drug reconstitution I IV Set attachment process.
Frequently asked questions
How many devices does Medimop Medical Projects, Ltd. have in the registry?
The registry currently lists 14 devices for Medimop Medical Projects, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medimop Medical Projects, Ltd.'s devices?
Among its 14 most recently registered devices, Medimop Medical Projects, Ltd. has devices listed in FDA 510(k) (14 devices).
What risk classes do Medimop Medical Projects, Ltd.'s devices fall under?
Among its 14 most recently registered devices, the classes recorded for Medimop Medical Projects, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Medimop Medical Projects, Ltd.?
FDA recall records list 1 recall initiated by Medimop Medical Projects, Ltd., the most recent initiated on 6 Oct 2017. 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 Medimop Medical Projects, Ltd. in the registry?
The most recently registered devices listed for Medimop Medical Projects, Ltd. include VIAL CONNECTOR 13MM CLOSED COLLAR, MODIFICATION TO MIXJECT DISPENSING PIN/WITH DETACHABLE VIAL HOLDER/WITH DETACHABLE VIAL HOLDER AND PRE-ATTACHED NEEDLE, MIX2VIAL TRANSFER DEVICE and Vial Adapter 15mm.