Devices

Ammonia Ultra Reagent

Model / Serial
List Number (LN): 6K89-30 Lot Number: 50083Y600 Expiration Date: 31 Jul 2016
Product Description
Reagent
Manufacturer
SENTINEL CH. SpA
1 Event
- translation missing: en.activerecord.attributes.event.titles.recall_field_safety_notice

Manufacturer

SENTINEL CH. SpA

Manufacturer Parent Company (2017)
Sentinel Ch. Spa
Manufacturers representative
Medical supplies & Services Co.Ltd Mediserv
Source
SFDA

3 devices with a similar name

Learn more about the data here

the Multigent Ammonia Ultra Reagent

Model / Serial
Product Description
In-vitro diagnostics - immunological products
Manufacturer
Sentinel CH. Spa

Sentinel MULTIGENT Ammonia Ultra Reagent

Model / Serial
Lot 50083Y600, expiration date 31 Jul 2016.
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: LN 6K89-30. Intended for the in vitro quantitative determination of Ammonia (NH3) in human plasma.
Manufacturer
Sentinel CH SpA

MULTIGENT Ammonia Ultra Reagent. An in vitro diagnostic medical device (IVD)

Model / Serial
MULTIGENT Ammonia Ultra Reagent. An in vitro diagnostic medical device (IVD)List Number: 6K89-30Lot Number: 50083Y600Expiration Date 31 Jul 2016ARTG Number: 203299
Manufacturer
Abbott Australasia Pty Ltd Diagnostic Division

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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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