Devices

AMPLIFIED MYCOBACTERIUM TUBERCULOSIS

Model / Serial
Product Description
in-vitro_medical_device
Manufacturer
BIO MERIEUX
1 Event
- Recall of AMPLIFIED MYCOBACTERIUM TUBERCULOSIS

Manufacturer

BIO MERIEUX

Source
LAANSM

2 devices with a similar name

Learn more about the data here

Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test, Catalog number 1001,

Model / Serial
Lots affected 305025 308126 309091 311067 308184 312083 403055 404065 405079 406083 406218 306299 308125 309092 308185 308124 310115 306150 309093 305165 311069 312146 401048 403054 403099 404084 406084 312146R 307177 305027 308183 3010378 311066 401104 403084 405074 307177B 305027B 308183B 310378B 305027C 311066B 311066C 401104B 403084B 405074B
Product Classification
Immunology and Microbiology Devices
Device Class
1
Implanted device?
No
Product Description
Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test, Catalog number 1001,
Manufacturer
Gen Probe Inc

GEN-PROBE AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT (MTD)TEST

Model / Serial
Model Catalog: (Lot serial: numerous)
Product Description
Gen-Probe Amplified MTD Test
Manufacturer
GEN-PROBE INCORPORATED DOING BUSINESS AS HOLOGIC 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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