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"Microscope Cover ZEISS ""MD"" 115/300 6.50 HLT"

Model 9296H · PHARMA SEPT MEDICAL PRODUCTS (1995) LTD. · DI 00836230000400

HRMMicroscope, Operating & Accessories, Ac-Powered, Ophthalmic · Class I · 21 CFR 878.4700

UDILibrary device dossier · generated 2026-09-06 · 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.

12342020-11: 0 reports for this device; peer average 1/device2021-03: 0 reports for this device; peer average 4/device2021-05: 0 reports for this device; peer average 1/device2021-06: 0 reports for this device; peer average 1/device2021-07: 0 reports for this device; peer average 1/device2021-08: 0 reports for this device; peer average 2/device2021-09: 0 reports for this device; peer average 1/device2021-12: 0 reports for this device; peer average 1/device2022-04: 0 reports for this device; peer average 1/device2022-06: 0 reports for this device; peer average 1/device2022-08: 0 reports for this device; peer average 2/device2023-04: 0 reports for this device; peer average 1/device2023-06: 0 reports for this device; peer average 2/device2023-07: 0 reports for this device; peer average 1/device2023-08: 0 reports for this device; peer average 1/device2023-12: 0 reports for this device; peer average 1.33/device2024-01: 0 reports for this device; peer average 1/device2024-02: 0 reports for this device; peer average 1/device2024-03: 0 reports for this device; peer average 2/device2024-06: 0 reports for this device; peer average 1/device2024-08: 0 reports for this device; peer average 1/device2024-12: 0 reports for this device; peer average 2/device2025-01: 0 reports for this device; peer average 2/device2025-03: 0 reports for this device; peer average 3/device2025-04: 0 reports for this device; peer average 1.5/device2025-05: 0 reports for this device; peer average 1/device2025-07: 0 reports for this device; peer average 1/device2025-10: 0 reports for this device; peer average 1/device2025-11: 0 reports for this device; peer average 1/device2025-12: 0 reports for this device; peer average 3/device2026-03: 0 reports for this device; peer average 1/device2026-04: 0 reports for this device; peer average 1/device1103050607080912040608040607081201020306081201030405071011120304
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2020-1101
2021-0304
2021-0501
2021-0601
2021-0701
2021-0802
2021-0901
2021-1201
2022-0401
2022-0601
2022-0802
2023-0401
2023-0602
2023-0701
2023-0801
2023-1201.33
2024-0101
2024-0201
2024-0302
2024-0601
2024-0801
2024-1202
2025-0102
2025-0303
2025-0401.5
2025-0501
2025-0701
2025-1001
2025-1101
2025-1203
2026-0301
2026-0401
This device (reports/month)Average device in HRM (reports/device/month)

Regulatory clearances

  • None linked in the loaded window.

Manufacturer compliance record — PHARMA SEPT MEDICAL PRODUCTS (1995) LTD.

Nothing in the loaded window.