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READYPAK

Beaver-Visitec International, Inc. · Model 58000609 · UDI-DI 30886158019504

PZG
0
510(k) clearances
4
Adverse events
6
Recalls
28
Facilities

Description

READYPAK KIT 58000609 (1/EA)

Recalls

DateFirmReason
2021-11-17Beaver Visitec International, Inc.Kit packaging may have small holes compromising product sterility
2021-11-17Beaver Visitec International, Inc.Kit packaging may have small holes compromising product sterility
2021-11-17Beaver Visitec International, Inc.Kit packaging may have small holes compromising product sterility
2021-11-17Beaver Visitec International, Inc.Kit packaging may have small holes compromising product sterility
2021-11-17Beaver Visitec International, Inc.Kit packaging may have small holes compromising product sterility
2021-11-17Beaver Visitec International, Inc.Kit packaging may have small holes compromising product sterility

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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.