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AESCULAP
Model MF363R · AESCULAP, INC. · DI 04046964571886
GDI — Dissector, Surgical, General & Plastic Surgery · Class I · 21 CFR 878.4800
UDILibrary device dossier · generated 2026-09-10 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (0)
No recalls linked in the loaded window.
Adverse-event reports — MAUDE (0)
Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-05
0
1
2019-08
0
1.67
2020-06
0
2
2020-08
0
6
2020-09
0
2
2020-11
0
4
2021-04
0
2
2022-05
0
6
2022-06
0
4
2022-07
0
4
2022-09
0
2
2022-10
0
3
2022-12
0
1
2023-01
0
2
2023-03
0
1
2023-04
0
1
2023-06
0
1
2023-07
0
3.25
2023-08
0
1.5
2023-09
0
1.67
2023-11
0
1.75
2024-01
0
1.67
2024-03
0
2.5
2024-04
0
2
2024-06
0
4
2024-08
0
22
2024-10
0
2.5
2024-11
0
1
2025-01
0
2.5
2025-02
0
1.67
2025-04
0
1.33
2025-05
0
1.5
2025-06
0
1
2025-07
0
2
2025-08
0
1
2025-09
0
2
2025-10
0
2
2025-11
0
3
2026-05
0
2
2026-06
0
2
This device (reports/month)Average device in GDI (reports/device/month)