SagiPlan® 2.x Software

2 catalogue numbers from 1374-0600#01, listed by Eckert & Ziegler Bebig Gmbh, Germany, under System, Planning, Radiation Therapy Treatment. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
2catalogue numbers in this listing
2510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (2), Fujian (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MUJ
Manufacturer City Province Registered as Device types
Philips Healthcare (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Manteia Technologies Co., Ltd. Xiamen Fujian Manufacturer 3
Masep Medical Science & Technology DEVELOPMENT(SHENZHEN)Co. Shenzhen Guangdong Manufacturer 2
Suzhou Linatech Medical Science AND Technology Co., Ltd. Suzhou Jiangsu Manufacturer 2
Varian Medical Systems China Co., Ltd. Beijing Beijing Manufacturer 2

Record

Regulatory record for SagiPlan® 2.x Software
Listed by Eckert & Ziegler Bebig Gmbh, Germany
FDA product code MUJ
Device type System, Planning, Radiation Therapy Treatment
Device class Class 2
Regulation 21 CFR 892.5050
Establishment Manufacturer
Record published 2016-10-07
Record revised 2024-02-29 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2024-02-28

Catalogue Numbers

Catalogue numbers for SagiPlan® 2.x Software
Catalogue number Size Status
1374-0600#01 Withdrawn
1374-0600#03 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
RayStation RaySearch Laboratories AB (publ) 29
System, Planning, Radiation Therapy Treatment Nucletron B.V. 17
Panther TPS Prowess, Inc. 14
RayCare RaySearch Laboratories AB (publ) 12
Accuray Precision® Treatment Planning System Accuray Incorporated 7
Monaco Elekta Inc. 7
Eclipse Treatment Planning System for External Beam Radiation Therapy Varian Medical Systems, Inc 6
syngo.via RT Image Suite Siemens Healthcare Limited 5
Eclipse Treatment Planning System Varian Medical Systems, Inc 5
Corvus 09 Best Nomos 4
Monaco Elekta Solutions AB 4
XKnife® Integra Lifesciences Corporation 4

Showing 12 of 98. All products under System, Planning, Radiation Therapy Treatment

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K141900 2015-05-20
K123263 2013-04-04

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2023-10-17 Class II Software Design Change Due to software malfunction, numerical values may be rounded resulting in inaccurate measurements. 2 software licenses in US, 255 software licenses in OUS

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer