Devices

OptiView Amplification Kit (250 Test)

Model / Serial
Model: 6718663001, Affected: Lot: Y19318
Product Classification
Hematology and Pathology Devices
Manufacturer
manufacturer #1479
1 Event
- Recall of OptiView Amplification Kit (250 Test)

Manufacturer

manufacturer #1479

Manufacturer Parent Company (2017)
Ivd Holdings Inc
Source
NZMMDSA

2 devices with a similar name

Learn more about the data here

Device Recall OptiView Amplification Kit (250 Test)

Model / Serial
UDI 04015630984749, Lot Numbers: Y19318
Product Classification
Hematology and Pathology Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide distribution, including US nationwide, Argentina, Australia, Hong Kong, Indonesia, Philippines, Brazil, Chile, Thailand, Korea, Malaysia, New Zealand, Ecuador, Mexico, Pakistan, Vietnam, Germany, Japan, India, Colombia, Singapore, Uruguay, Peru, Canada, Taiwan, China,
Product Description
OptiView Amplification Kit (250 Test), Ventana Part Number 860-099, Roche GMMI 06718663001 in vitro diagnostic
Manufacturer
Ventana Medical Systems Inc

OptiView DAB IHC Detection Kit, ultraView Universal DAB Detection Kit, ultraView Universal DAB De...

Model / Serial
Catalog Number: viz FSN Batch Number: viz FSN
Product Description
Diagnostic medical devices in vitro
Manufacturer
Ventana Medical Systems Inc

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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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