Collimator, Automatic, Radiographic
Radiology · 21 CFR 892.1610
Recent MDR events
9 adverse event reports on file
- COLLIMATOR, AUTOMATIC, RADIOGRAPHICDec 13, 2024MalfunctionSiemens Healthineers1000513161-2024-00039
- MIDMARK/PROGENYSep 17, 2014MalfunctionQuantum Medical Imaging, Llc.2438474-2014-00002
- EUREKA COLLIMATORJun 23, 2011MalfunctionMidmark Corporation1423380-2011-00002
- EUREKA COLLIMATORJan 22, 2010MalfunctionMidmark Corporation1423380-2009-00031
- LINGAR COLLIMATORJul 2, 2007MalfunctionProgeny, Inc889514
- ULTRANET SMay 30, 2007MalfunctionGe Medical Systems S.c.s.9611343-2007-00043
- RALCO COLLIMATOR IN XPLORER 1590 SYSTEMNov 27, 2006MalfunctionRalco Inc9616853-2006-00003
- LINEAR IIIMar 19, 2002MalfunctionProgeny, Inc.1423380-2002-00001
- EUREKA LINEAR IIINov 8, 2000InjuryProgeny, Inc.1423380-2000-00001
Event type breakdown
Recalls
3 recall events for this product code
- Shimadzu Medical SystemsTerminatedNov 8, 2012
R-30H , Diagnostic X-Ray Beam-Limiting Device.
Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray system and Diagnostic x-ray tube assembly because they do not comply with the Product Performance Standards, 21CFR 1020.30 (m) Beam quality --(1) Half-value layer (HVL), which was revised in 2006. Certain devices might not comply with the requirements for them in some x-ray generating condition after the revision in 2006.
Z-0260-2013 · View FDA record ↗ - Philips Medical Systems North America Co. PhillipsTerminatedSep 16, 2008
Philips Gallileo Automatic Collimator, Part Numbers: 9896 010 00612, 9896 010 00614, 9896 010 00615. The device is a diagnostic x-ray beam-limiting device inte
The collimator could fall from the x-ray stand, due to loosening screws, and strike a patient or operator underneath.
Z-1886-2008 · View FDA record ↗ - Philips Medical Systems North America Co. PhillipsTerminatedJun 14, 2007
Philips Collimators, Model numbers: 9896 010 00614, 9896 010 00615, 9804 607 00301, and 9804 602 83501. Product is a Collimator/ Beam Limiting Device and are r
The Collimator field-defining light beam does not meet the light field contrast ratio requirement of 4:1. System is non-compliant with performance standard (1020.31 (d)(2)(iii) 21 CFR
Z-0739-2007 · View FDA record ↗
Registered firms
26 firms currently registered for this product code
Ge Healthcare (china) Co., Ltd.
Beijing, CN
Suzhou Shangchuang Technology Service Co., Ltd.
Suzhou Jiangsu, CN
Philips Electronics Ltd
Mississauga Ontario, CA
Fairy Medical Electrics(jiaxing)co.,ltd
Jiaxing Zhejiang, CN
Philips Medical Systems Nederland B.v.
BEST Noord-Brabant, NL
Ge Medical Systems Monterrey Mexico, S.a. De C.v.
APODACA Nuevo Leon, MX
Del Medical, Inc.
Bloomingdale, IL, US
Ge Medical Systems Ultrasound & Primary Care Diagnostics Llc
MADISON, WI, US
Philips Medical Systems Nederland B.v.
BEST Noord-Brabant, NL
Ge Medical Systems, Llc
Waukesha, WI, US
Ralco S.r.l.
Biassono Monza e Brianza, IT
Ge Hangwei Medical Systems Co., Ltd.
Beijing, CN
Dhl Supply Chain (netherlands) B.v.
Beringe Limburg, NL
Makar Consulting Pty Ltd
Belrose New South Wales, AU
Shimadzu Corporation Medical Systems Division
KYOTO, JP
Agito Medical
Norresundby Nordjylland, DK
Iray Imaging Technology (haining) Limited
Haining Zhejiang, CN
510(k) clearances
23 clearances for this product code
- Shimadzu Corp.Sep 20, 2010
K101039 · SHIMADZU COLLIMATOR R-300
- Omega Medical Imaging, Inc.Feb 3, 2010
K093572 · R650 QDASM COLLIMATOR
- Shimadzu Corp.Nov 6, 2009
K090578 · SHIMADZU COLLIMATOR R-30H
- Ralco S.R.L.Jul 14, 2009
K091517 · RALCO, MODEL R225 ACS
- Ralco S.R.L.Dec 5, 2008
K083029 · MODEL R605DASM AUTOMATIC X-RAY COLLIMATOR
- Ralco S.R.L.Nov 26, 2007
K072780 · MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR
- Collimare, LLCNov 16, 2007
K073124 · COLLIMARE COLLIMATOR FAMILY
- Omega Medical Imaging, Inc.Jan 31, 2005
K050092 · R605 FACS COLLIMETER