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i.Series®

HELMER, INC. · Model iLR105 · UDI-DI 00816394020193

KSE
4
510(k) clearances
383
Adverse events (3 deaths)
0
Recalls
38
Facilities

Description

Laboratory/Pharmacy Refrigerator - Undercounter, 5 cu ft

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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.