Print-ready dossier — use your browser's print dialog to save as PDF.
Aquilex® Fluid Control System
Model AQL-100CS · W.O.M. World of Medicine GmbH · DI 04056702002145
HIG — Insufflator, Hysteroscopic · Class II · 21 CFR 884.1700
UDILibrary device dossier · generated 2026-09-11 · 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 (31)
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.
Malfunction: 30 · Death: 1
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-01
0
2
2019-02
0
4
2019-03
0
3
2019-04
0
6.5
2019-05
2
2.33
2019-06
2
4.25
2019-07
0
2
2019-08
2
2
2019-09
0
4
2019-10
2
2.4
2019-11
2
2
2019-12
2
1.8
2020-01
0
1.5
2020-02
0
1.5
2020-03
0
2.33
2020-04
2
2
2020-05
0
1.33
2020-07
0
2
2020-08
2
1.67
2020-09
0
1.5
2020-10
0
2.2
2020-11
0
1
2020-12
0
2
2021-02
0
7
2021-03
2
6.67
2021-04
0
3
2021-05
0
2.5
2021-06
2
12.25
2021-07
0
22.5
2021-08
0
16.5
2021-09
0
8.5
2021-10
0
30
2021-11
0
22
2021-12
2
11.75
2022-01
0
12.67
2022-02
0
9
2022-03
0
34
2022-04
6
3.25
2022-05
0
3
2022-06
0
1.67
2022-07
0
3
2022-08
0
2
2022-09
0
4
2022-10
0
2
2022-11
0
2
2022-12
0
2
2023-02
0
2.67
2023-03
0
3
2023-04
0
2
2023-05
2
2.33
2023-06
0
2.5
2023-07
0
3
2023-08
1
1.67
2023-09
0
2.75
2023-10
0
2
2023-11
0
3
2023-12
0
2.33
2024-01
0
3.5
2024-02
0
3.5
2024-03
0
2
2024-04
0
3.25
2024-05
0
2
2024-06
0
2.33
2024-07
0
3.5
2024-08
0
1.67
2024-09
0
1.5
2024-10
0
5
2024-11
0
6.67
2024-12
0
4
2025-01
0
1.6
2025-02
0
3.5
2025-03
0
3
2025-04
0
1
2025-05
0
3
2025-06
0
1.8
2025-07
0
5
2025-09
0
1.5
2025-10
0
2.83
2025-11
0
3
2025-12
0
2
2026-01
0
2
2026-02
0
2.5
2026-03
0
3.2
2026-04
0
2
2026-05
0
1.25
2026-06
0
3.83
This device (reports/month)Average device in HIG (reports/device/month)
Regulatory clearances
K112642 SESE 2012-02-06 (k number procode)
Predicate lineage
K112642 — cites (transitively): K031616 (d1), K062380 (d1), K936231 (d1) — cited as predicate by K172040, K173489, K180825
Lineage extracted from public 510(k) summary text (heuristic).
Manufacturer compliance record — W.O.M. World of Medicine GmbH