FDA Device Intelligence
Home › MAVIG GmbH › RP

RP

MAVIG GmbH · Model RP6435L22SB12-PH · UDI-DI 04251339906259

IWOEAJ
1
510(k) clearances
5
Adverse events
13
Recalls
80
Facilities

Description

RP - Radiation Protective Clothing Patient Gonad Apron Model RP643-STD

Recalls

DateFirmReason
2026-02-11Burlington Medical, LLCPotential for attenuation degradation over time, decreasing the lifespan.
2026-02-11Burlington Medical, LLCPotential for attenuation degradation over time, decreasing the lifespan.
2026-02-11Burlington Medical, LLCPotential for attenuation degradation over time, decreasing the lifespan.
2026-02-11Burlington Medical, LLCPotential for attenuation degradation over time, decreasing the lifespan.
2026-02-11Burlington Medical, LLCPotential for attenuation degradation over time, decreasing the lifespan.
2026-02-11Burlington Medical, LLCPotential for attenuation degradation over time, decreasing the lifespan.
2026-02-11Burlington Medical, LLCPotential for attenuation degradation over time, decreasing the lifespan.
2026-02-11Burlington Medical, LLCPotential for attenuation degradation over time, decreasing the lifespan.
2026-02-11Burlington Medical, LLCPotential for attenuation degradation over time, decreasing the lifespan.
2026-02-11Burlington Medical, LLCPotential for attenuation degradation over time, decreasing the lifespan.

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.