FDA Device Intelligence
Home › CHROMA ATE INC. › CHROMA ATE

CHROMA ATE

CHROMA ATE INC. · Model MagXtract 3200 · UDI-DI 04719889100010

JJH
10
510(k) clearances
295
Adverse events (1 deaths)
31
Recalls
99
Facilities

Description

MagXtract 3200 Automated Nucleic Acid Extraction System The MagXtract 3200 system is an automated nucleic acid purification and PCR reaction preparation system consisting of MagXtract 3200 instrument, software and consumables. It must be used in combination with the authorized extraction kits which have been validated according to the IVD or other relevant regulations to perform the nucleic acid purifications. The MagXtract 3200 System is intended for use by professional users for the purification of nucleic acids and PCR sample prep from human samples for in vitro diagnostic purposes. Product Use Limitations: The MagXtract 3200 instrument is intended for indoor use only. The user is responsible for establishing performance characteristics necessary for downstream diagnostic applications. Appropriate controls must be included in any downstream diagnostic applications using nucleic acids, purified by the instruments.

Recalls

DateFirmReason
2024-06-03Qiagen Sciences LLCHeater shaker module does not perform heating if the temperature is set below 40C for static incubation steps when running IVD protocol QIAamp DSP DNA Mini Kit (cat. no. 61304), Pr
2024-03-04Qiagen Sciences LLCInsufficient welding leads to the heater cable becoming brittle and present with an error: ERROR 3481 HEATER UNABLE TO REACH TEMPERATURE; the instrument may stop, and the sample b
2023-02-21Entopsis , Inc.Presence of misleading label statements on the product label.
2023-02-21Entopsis , Inc.Presence of misleading label statements on the product label.
2023-02-21Entopsis , Inc.Presence of misleading label statements on the product label.
2023-02-21Entopsis , Inc.Presence of misleading label statements on the product label.
2023-02-21Entopsis , Inc.Presence of misleading label statements on the product label.
2023-02-21Entopsis , Inc.Presence of misleading label statements on the product label.
2023-02-21Entopsis , Inc.Presence of misleading label statements on the product label.
2022-11-02Qvella CorporationDevice exceeds the limitations of a Class I 510(k)-exempt device so the user manual, instructions for use, and promotional materials are being corrected to remove all references to

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.