International Medical Devices Database

Manufacturer Address
TRENTO
Source
HC
1 Event
- Recall of HAND-HELD SPOT PROBE

One device in the database

HAND-HELD SPOT PROBE

Model / Serial
Model Catalog: HAND-HELD SPOT (Lot serial: CONTACT MANUFACTURER); Model Catalog: INTENSIVE PAD (Lot serial: CONTACT MANUFACTURER); Model Catalog: SMART (Lot serial: CONTACT MANUFACTURER); Model Catalog: FIELD INCREASERS (Lot serial: CONTACT MANUFACTURER); Model Catalog: MED (Lot serial: CONTACT MANUFACTURER); Model Catalog: FAM (Lot serial: CONTACT MANUFACTURER); Model Catalog: HC (Lot serial: CONTACT MANUFACTURER)
Product Description
HAND-HELD SPOT PROBE;PRO INTENSIVE APPLICATOR;SMART SEQEX;FIELD ENHANCEMENT SET;SEQEX MED;SEQEX FAM;SEQEX HC;HOME UNIT INTENSIVE APPLICATOR

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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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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SISTEMI SRL

One device in the database

HAND-HELD SPOT PROBE