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Devices
Device Recall Dr. Landi EVLT Pack
모델명 / 제조번호(시리얼번호)
Lot number and expiration date 100007, 2/26/2019 100008, 2/3/2019 100009, 2/10/2019 100322, 4/2/2019 101129, 2/21/2019 84854, 12/26/2017 85111, 12/1/2017 86047, 12/19/2017 86791, 5/7/2018 88616, 5/13/2018 88617, 6/11/2018 88845, 6/12/2018 89076, 10/22/2018 89175, 10/7/2018 89568, 11/9/2018 89715, 11/25/2018 94567, 10/23/2018 97120, 12/7/2018 97562, 11/27/2018 97771, 11/27/2018 98014, 11/11/2018 98014, 11/11/2018 98160, 2/22/2018 98161, 11/21/2018 98162, 11/30/2018 98494, 2/13/2019
의료기기 분류등급
General and Plastic Surgery Devices
의료기기 등급
2
이식된 장치?
No
유통
Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.
제품 설명
Dr. Landi EVLT Pack, part number AMS1483(E || Dr. Landi EVLT Pack, part number AMS1483(E
Manufacturer
Windstone Medical Packaging, Inc.
1 Event
Device Recall Dr. Landi EVLT Pack 의 리콜
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제조사
Windstone Medical Packaging, Inc.
제조사 주소
Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
제조사 모회사 (2017)
Windstone Medical Packaging Inc.
Source
USFDA
Language
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