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IM-HD1TVM

NARISHIGE LIFEMED CO., LTD. · Model IM-HD1TVM Pneumatic Microinjector · UDI-DI 04589818020128

MQJ Prescription
10
510(k) clearances
2
Adverse events
1
Recalls
12
Facilities

Description

Assisted Reproduction Microinjector

Recalls

DateFirmReason
2016-03-11RESEARCH INSTRUMENTS LTD - SITE BThe units have been fitted with a potentially faulty power supply cable.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.