Devices

cobas 4800 HPV Amplification/Detection Kit

Model / Serial
Model: , Affected: Lot numbers X10763, X09600, X13438, Y00444
Manufacturer
Roche SAS
1 Event
- Recall of cobas 4800 HPV Amplification/Detection Kit

Manufacturer

Roche SAS

Manufacturer Parent Company (2017)
Roche Holding AG
Source
NZMMDSA

3 devices with a similar name

Learn more about the data here

COBAS 4800 HPV AMPLIFICATION/DETECTION KIT

Model / Serial
Model Catalog: 05235901190 (Lot serial: > than 10 contact MFR); Model Catalog: 05235910190 (Lot serial: > than 10 contact MFR)
Product Description
COBAS 4800 HPV AMPLIFICATION/DETECTION KIT
Manufacturer
ROCHE DIAGNOSTICS

COBAS 4800 HPV AMPLIFICATION/DETECTION KIT

Model / Serial
Model Catalog: 05235901190 (Lot serial: R15771); Model Catalog: 05235910190 (Lot serial: R15304); Model Catalog: 05235901190 (Lot serial: R15304); Model Catalog: 05235910190 (Lot serial: R15771)
Product Description
COBAS 4800 HPV AMPLIFICATION/DETECTION KIT
Manufacturer
ROCHE DIAGNOSTICS

cobas 4800 HPV Amplification/Detection Kit. An in vitro diagnostic medical device (IVD)

Model / Serial
cobas 4800 HPV Amplification/Detection Kit. An in vitro diagnostic medical device (IVD)Material Numbers: 05235910190 and 05235901190Pack Size: 960 and 240 tests (respectively)Multiple Lot NumbersARTG Number: 187190
Manufacturer
Roche Diagnostics Australia Pty Limited

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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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