Macromedics BV
Netherlands NL-MF-000006068 Last updated 25 Oct 2026
- Devices
- 481
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
Mask TSRSO3-HO set/10 Ref 369140
Mask LMPFC-3P set/10 Ref 139535
Couchtop Ref 142410
Couchtop Ref 142120
Mask LMCF-5P set/10 Ref 119555
Mask ELMCF-L set/10 Ref 132220
DSPS® Cradle-M H RE MR Ref 171250
Couchtop Ref 140340
Low Bridge Support, RE, MR Ref 173540
ThoraxSupport™ short Ref 122650
Handgrips RE or TS, MRC, right Ref 111280R
Prone Tool Mouldroom DSCP™ Ref 173570
Mask MCFC-5 set/10 Ref 117450
FlexBoard™ LX package Ref 173630
Couchtop Ref 140450
Upper AS TS/MBLX, MRC, set/2 Ref 122310
Mask DSPS®-FSOSL, set/5 Ref 114570
EagleBoard™-2 M-Grip&Adaptor HS Ref 122900
DSPS® Cradle-U H Ref 112770
Armcup for handpoles right Ref 122740R
OmniBoard™ BTM-LX Ref 173600
Mask REMCF-13 set/10 Ref 359630
MaxSupport™ MR set/3 Ref 116205
FlexBoard™ SX package RAS Ref 172500
Couchtop Ref 140120
Mask REMCF-3 set/10 Ref 359530
Handpoles with armcup, set/2 Ref 122760
EagleBoard™-2 Adaptor OB RE/TS Ref 123010
SSPS™ Cradle RE Ref 111120
DSPS-Prominent® Cradle-VI Ref 113180
Mask OWLMCF-3 set/10 Ref 129630
Breast Treatment Module LX, MRC Ref 173650
DSPS-Prominent® Cradle-III Ref 113160
ExaFix Ref 111770
Mask DSPS®-FSOPS, set/5 Ref 114340
ExaFix Ref 111720
Mask TURS3 set/10 Ref 374430
Handpole MBLX-LB1 Ref 122730U
MaxSupport™ S-BC Ref 116520
Wedges, CF, set/3 Ref 110700
Eamis lite™ system 123800 Ref 123800
Profiles LB1, set/2 Ref 122390
Mask LMPFC-3 set/10 Ref 139530
Mask TSRCS3-HNS set/10 Ref 369490
Mask REMCF-12 set/10 Ref 359620
Couchtop Ref 142340
BreastBoardSX™, RAS Ref 172400
LEPS™ FeetSupport™, fixed Ref 130310
Mask TSRPNR3-HNS set/10 Ref 363470
Couchtop Ref 142440
Showing 201-250 of 481
What Macromedics BV makes
Macromedics BV manufactures patient positioning devices for medical imaging, including adjustable boards like the FlexBoard™ and EagleBoard™, as well as specialized breast positioning supports such as the BreastBoard SXTM. The company also produces vacuum cushions, foot supports, and lower extremity positioning systems (LEPS) to enhance patient comfort and stability during procedures. Additional products include modular DSPS-Prominent® baseplates and cradles designed for MRI compatibility, along with various DSPS-Prominent® mask sets for precise head immobilization.
The company’s portfolio consists of Class II medical devices, regulated under the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, reflecting their compliance with U.S. medical device regulations. Macromedics BV is based in the United States.
Frequently asked questions
What types of medical devices does Macromedics BV manufacture?
Macromedics BV specializes in patient positioning devices primarily used in medical imaging. Their portfolio includes adjustable positioning boards like the FlexBoard™ and EagleBoard™, specialized breast supports such as the BreastBoard SXTM, vacuum cushions, foot supports, and lower extremity positioning systems (LEPS) to improve patient stability and comfort. They also offer modular DSPS-Prominent® baseplates and cradles, some designed for MRI compatibility, along with mask sets for head immobilization during procedures.
Where is Macromedics BV based?
Macromedics BV is based in the United States. The company’s headquarters and operations are located within the country, aligning with its focus on manufacturing and distributing medical devices regulated by U.S. authorities.
Which regulatory registries list Macromedics BV’s devices?
Macromedics BV’s devices are listed in the FDA’s 510(k) registry. This registry includes Class II medical devices that have undergone the FDA’s 510(k) clearance process, demonstrating compliance with U.S. medical device regulations. The inclusion in this registry reflects the authorization status of individual devices rather than the company itself.
How are Macromedics BV’s devices classified under U.S. regulations?
Macromedics BV’s devices fall under Class II classification according to U.S. medical device regulations. Class II devices generally pose moderate risk and require special controls in addition to general controls to ensure their safety and effectiveness. These devices must comply with the FDA’s 510(k) clearance process before being marketed.
Information
- Country
- Netherlands
- Address
- 670, Oostbaan, Moordrecht, Netherlands
- Website
- www.macromedics.com
- [email protected]
- Phone
- +31 (0)1 82 38 97 77
- PRRC contact
- Elizabeth Hajós
- EUDAMED SRN
- NL-MF-000006068
- FDA FEI number
- 3010701021