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FAQ
Crédits
Devices
Device Recall Peregrine 20 GA Endo Ocular Adjustable Laser Probe (Smart Flex)
Modèle / numéro de série
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.
Classification du dispositif
Ophthalmic Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Product was distributed to hospitals and eye surgery centers in Florida, Maryland, Missouri, North Carolina, Ohio, Pennsylvania, Texas.
Description du dispositif
Peregrine 20 GA Endo Ocular Adjustable Laser Probe
Manufacturer
Peregrine Surgical Ltd
1 Event
Rappel de Device Recall Peregrine 20 GA Endo Ocular Adjustable Laser Probe (Smart Flex)
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Fabricant
Peregrine Surgical Ltd
Adresse du fabricant
Peregrine Surgical Ltd, 51 Britain Dr, New Britain PA 18901-5186
Société-mère du fabricant (2017)
Peregrine Surgical Ltd.
Source
USFDA
Language
English
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