Devices

Device Recall NAMIC (TM) Convenience Kit

Model / Serial
Lots 4693027, 4693271, 4693804, 4701037, 4705269, 4728884, 4733063, 4750828, 4764547, 4770885, 4779423, 4816850, 4822738, 4829934.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.
Product Description
NAMIC Convenience Kit, UPN H749602001451, REF/Catalog No. 60200145, STERILE, Rx ONLY ---For single use only. --- Device Listing Number D136588. || NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
Manufacturer
Navilyst Medical, Inc
1 Event
- Recall of Device Recall NAMIC (TM) Convenience Kit

Manufacturer

Navilyst Medical, Inc

Manufacturer Address
Navilyst Medical, Inc, 10 Glens Falls Technical Park, Glens Falls NY 12801
Manufacturer Parent Company (2017)
Navilyst Medical, Inc
Source
USFDA

58 devices with a similar name

Learn more about the data here

Device Recall NAMIC (TM) Convenience Kit

Model / Serial
Lot 4256783, 4460497, 4575427, 4582488, 4638692, 4656910.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.
Product Description
NAMIC Convenience Kit, LEFT HEART KIT, UPN H749602000571, REF/Catalog No. 60200057, STERILE, Rx ONLY --- For single use only. || --- Device Listing Number D136588. || NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
Manufacturer
Navilyst Medical, Inc

Device Recall NAMIC (TM) Convenience Kit

Model / Serial
Lot 4399506
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.
Product Description
NAMIC Convenience Kit, UPN H749606204751, REF/Catalog No. 60620475, STERILE, Rx ONLY --- For single use only. --- Device Listing Number D136588. || NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
Manufacturer
Navilyst Medical, Inc

Device Recall NAMIC (TM) Convenience Kit

Model / Serial
Lot 4440346
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.
Product Description
NAMIC Convenience Kit, LEFT HEART KIT, UPN H965600125911, REF/Catalog No. 60012591, STERILE, Rx ONLY ---For single use only. --- Device Listing Number D136588. || NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
Manufacturer
Navilyst Medical, Inc

Device Recall NAMIC (TM) Convenience Kit

Model / Serial
Lots 4600293, 4604109, 4630591, 4638147, 4643561, 4651008, 4798764, 4805945.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.
Product Description
NAMIC Convenience Kit, UPN H965600338021, REF/Catalog No. 60033802, STERILE, Rx ONLY ---For single use only. --- Device Listing Number D136588. || NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
Manufacturer
Navilyst Medical, Inc

Device Recall NAMIC (TM) Convenience Kit

Model / Serial
Lots 4323681, 4398529, 4699521.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.
Product Description
NAMIC Convenience Kit, LEFT HEART KIT, UPN H965600416321, REF/Catalog No. 60041632, STERILE, Rx ONLY --- For single use only. --- Device Listing Number D136588. || NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
Manufacturer
Navilyst Medical, Inc

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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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