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SU-VEID

ANGIE TECHNOLOGIES LTD · Model 18103300 · UDI-DI 07290018896235

FRF Prescription
1
510(k) clearances
31
Adverse events
1
Recalls
11
Facilities

Description

Carton of 16 boxes (DI# 07290018896136) of 30 SU-VEID units each (DI# 07290018896037) - for a total of 480 SU-VEID units per carton.

Recalls

DateFirmReason
2012-01-09Healthway Home Products, Inc.The Company is recalling certain serial numbers of HealthWay Model 20600-3 and CleanStation Model CS20000 air purifiers because of a potential risk of electrical arcing that could

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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.