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Device, Rebreathing

FDA product code BYW · Class 1 · Anesthesiology

14
Registered devices
29
Adverse events
1
Recalls
2
510(k) clearances

Devices with this code

MTEHFYAF — Beijing Xingjian Yongzhen Technology Co. , Ltd.n.a. — VBM Medizintechnik GmbHANEclear — ANECARE, LLCMonaghan Medical Corporation — Monaghan Medical CorporationPaediatric Mask; Newborn — VBM Medizintechnik GmbHPaediatric Mask; Child — VBM Medizintechnik GmbHMTEHFYAF — Beijing Xingjian Yongzhen Technology Co. , Ltd.MedSource Rebreather Mask — MEDSOURCE INTERNATIONAL LLCMTEHFYAF — Beijing Xingjian Yongzhen Technology Co. , Ltd.MedSource Rebreather Mask — MEDSOURCE INTERNATIONAL LLCAE II BAN — Monaghan Medical Corporationn.a. — VBM Medizintechnik GmbHn.a. — VBM Medizintechnik GmbHPaediatric Mask; Infant — VBM Medizintechnik GmbH

Recent recalls

DateFirmReason
2006-10-31Teleflex MedicalMislabeling-The rebreathing bag is incorrectly labeled as a 1 liter bag when it is actually a 1/2 liter bag.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.