FDA Device Intelligence
HomeDevice types › JRC

Micro Pipette

FDA product code JRC · Class 1 · Clinical Chemistry

1,042
Registered devices
4
Adverse events
3
Recalls
6
510(k) clearances

Devices with this code

ASSY,Reag.Disp.Card,PrepKit 120,BenchMar — Ventana Medical Systems, Inc.Pipette tip 1000 µl — Sarstedt Aktiengesellschaft & Co.KGGlobe Scientific — GLOBE SCIENTIFIC INC.Pipette tip 300 µl — Sarstedt Aktiengesellschaft & Co.KGASSY,Reag.Disp.Card, BMK Prep Kit 501 — Ventana Medical Systems, Inc.ASSY,Reag.Disp.Card,PrepKit 94,BenchMark — Ventana Medical Systems, Inc.Reag.Disp.Card,Prep Kit 2,250-Series Test — Ventana Medical Systems, Inc.Filter tip 200 µl — Sarstedt Aktiengesellschaft & Co.KGASSY,Reag.Disp.Card,PrepKit 98,BenchMark — Ventana Medical Systems, Inc.ASSY,Reag.Disp.Card,PrepKit 39,BenchMark — Ventana Medical Systems, Inc.Reag.Disp.Card,Prep Kit 33,250-Series Test — Ventana Medical Systems, Inc.ASSY RGT DSPNR CARD BMK PREP KIT 234 — Ventana Medical Systems, Inc.Pipette tip 1000 µl — Sarstedt Aktiengesellschaft & Co.KGGlobe Scientific — GLOBE SCIENTIFIC INC.Globe Scientific — GLOBE SCIENTIFIC INC.Globe Scientific — GLOBE SCIENTIFIC INC.Light Protective Prep Kit — Ventana Medical Systems, Inc.ASSY,Reag.Disp.Card, BMK Prep Kit 507 — Ventana Medical Systems, Inc.Reag.Disp.Card,Prep Kit 35,250-Series Test — Ventana Medical Systems, Inc.ASSY,Reag.Disp.Card,PrepKit 89,BenchMark — Ventana Medical Systems, Inc.Reag.Disp.Card,Prep Kit 84,250-Series Test — Ventana Medical Systems, Inc.ASSY,Reag.Disp.Card, BMK Prep Kit 509 — Ventana Medical Systems, Inc.Reag.Disp.Card,Prep Kit 150,250-Series Test — Ventana Medical Systems, Inc.Pipette tip — Sarstedt Aktiengesellschaft & Co.KG

Recent recalls

DateFirmReason
2023-07-14Copan Diagnostics IncDue to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance
2022-05-25Mckesson Medical-Surgical Inc. Corporate OfficeFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lot
2021-12-10Ortho-Clinical Diagnostics, Inc.The lot has a shape deformity which may lead to a 16% reduction in the volume of the sample or reagent dispensed. In cases where the error is not detected and t

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.