Devices

Device Recall Suction Regulator

Model / Serial
Regulator Model 7702L, Lot Number 04D
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
The recalled product was distributed to the following states: AL, FL, MA, MI, OR, PA, TN,
Product Description
Boheringer Suction Regulator Model 7702L, Lot number 04D || Boehinger Replacement Gauge, Model 9071, Lot number 200405.
Manufacturer
Boehringer Laboratories Inc
1 Event
- Recall of Device Recall Suction Regulator

Manufacturer

Boehringer Laboratories Inc

Manufacturer Address
Boehringer Laboratories Inc, 500 E Washington St, Norristown PA 19401-5149
Source
USFDA

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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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