International Medical Devices Database

Manufacturer Address
Peregrine Surgical Ltd, 51 Britain Dr, New Britain PA 18901-5186
Manufacturer Parent Company (2017)
Peregrine Surgical Ltd.
Source
USFDA
1 Event
- Recall of Device Recall Peregrine 20 GA Endo Ocular Adjustable Laser Probe (Smart Flex)

One device in the database

Device Recall Peregrine 20 GA Endo Ocular Adjustable Laser Probe (Smart Flex)

Model / Serial
Device numbers: PD720.50, PD720.52, PD723.50, PD723.52, PD725.50, PD725.52. Lot numbers 926287, 937391, 931335, 933355, 935370, 937390, 940422, 916188, 917184, 919211, 920228, 922244, 925269, 916189, 917185, 919216, 920229, 923245, 925272, 952026, 002048, 005069, 916186, 918196, 919205, 920240, 924268, 926285, 916184, 918203, 919208, and 922239.
Product Classification
Ophthalmic Devices
Device Class
2
Implanted device?
No
Distribution
Product was distributed to hospitals and eye surgery centers in Florida, Maryland, Missouri, North Carolina, Ohio, Pennsylvania, Texas.
Product Description
Peregrine 20 GA Endo Ocular Adjustable Laser Probe

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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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Peregrine Surgical Ltd

One device in the database

Device Recall Peregrine 20 GA Endo Ocular Adjustable Laser Probe (Smart Flex)