International Medical Devices Database

Manufacturer Parent Company (2017)
Baxter International
Source
SATP
1 Event
- Field Safety Notices about Polyflux Revaclear / Polyflux Revaclear Max

One device in the database

Polyflux Revaclear / Polyflux Revaclear Max

Model / Serial
110633 / 110634 | C413104001, C413104201, C413104301, C413105401, C413105901, C413106601, C412207201, C412207401, C412207701, C412207901, C412208001, C412208401, C412208501, C412208801, C412208901
Product Description
MD: Hollow-fibre haemodialysis dialyser, high flux, single-use

4 manufacturers with a similar name

Learn more about the data here

Gambro Renal Products, Inc.

Manufacturer Parent Company (2017)
Baxter International
Source
NIDFSINVIMA

Nipro Corporation || Quintin Instrument Co || Baxter Healthcare Corporation Of Puerto Rico || Alt...

Source
NIDFSINVIMA

Gambro Renal Products, Inc.

Manufacturer Address
Gambro Renal Products, Inc., 10810 W Collins Ave, Lakewood CO 80215-4439
Source
USFDA

Gambro Renal Products, Inc.

Manufacturer Address
Gambro Renal Products, Inc., 14143 Denver West Pkwy, Lakewood CO 80401-3116
Manufacturer Parent Company (2017)
Baxter International
Source
USFDA

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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