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Apatech Ltd

1 inspections · aggregated across 2 source records

Scorecard
Events per device across the 43-device portfolio, trailing 12 months. Arrows compare the last 90 days with the 90 before.

MAUDE reports per device

0

0 in the last 12 months

Higher volume than 83% of companies with 10+ devices

Recalls per device

0

0 in the last 12 months

Higher volume than 97% of companies with 10+ devices

These are reporting-volume percentiles, not safety rankings — MAUDE counts have no denominator of devices in use, and recall attribution follows resolved links. A high percentile means more reports per registered device than peers, which can reflect market size, device criticality, or reporting practice as much as anything else.

Devices
43 device records · ordered by linked event volume.
BrandModelProduct codesPrimary DILinked events
ALTAPORE1508032MQV000854126307311
ALTAPORE1508047MQV000854126781461
Actifuse Flow506005078077MQV050600507807771
Actifuse Flow506005078076MQV050600507807601
Actifuse Flow506005078078MQV050600507807841
Actifuse Shape506005078068LYC MQV050600507806851
ACTIFUSE ABX0
ACTIFUSE E-Z-PREP0
ACTIFUSE GRANULES0
ACTIFUSE MICROGRANULES0
ACTIFUSE MIS SYSTEM0
ACTIFUSE MIS SYSTEM REFILL CARTRIDGE0
ALTAPORE1504323MQV054137604790020
ALTAPORE1504321MQV054137604789820
ALTAPORE1504319MQV054137604789680
ALTAPORE1504322MQV054137604789990
ALTAPORE1508045MQV000854126543790
ALTAPORE1504320MQV054137604789750
ALTAPORE1508043MQV000854126543930
ALTAPORE1508044MQV000854126543860
ALTAPORE1508046MQV000854126543620
Actifuse ABX506005078050LYC MQV050600507805000
Actifuse ABX506005078051LYC MQV050600507805170
Actifuse ABX506005078052LYC MQV050600507805240
Actifuse ABX506005078058LYC MQV050600507805860
Actifuse ABX506005078060LYC MQV050600507806090
Actifuse E-Z-Prep506005078054LYC MQV050600507805480
Actifuse Granules506005078030LYC MQV050600507803020
Actifuse Granules506005078029LYC MQV050600507802960
Actifuse Granules506005078028LYC MQV050600507802890
Showing 1–30 of 43Next →
Facilities
Registered establishments with their latest FDA inspection outcome.

No registered facilities linked.