International Medical Devices Database

Manufacturer Address
Gen Probe Inc, 10210 Genetic Center Dr, San Diego CA 92121-4362
Source
USFDA
1 Event
- Recall of Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test, Catalog number 1001,

One device in the database

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,

One manufacturer with a similar name

Learn more about the data here

Gen Probe Incorporated

Manufacturer Parent Company (2017)
Grifols Sa
Manufacturers representative
Al-Jeel Medical & Trading Co. Ltd, Riyadh, (01) 4041717
Source
SFDA

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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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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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