Macromedics BV
Netherlands NL-MF-000006068 Last updated 25 Oct 2026
- Devices
- 481
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
Mask DSPS®-FOSVR, set/5 Ref 114410
FluxBoard Ref 164140
FlexBoard™ EX + EagleBoard-2 Package Ref 172150
MaxSupport™ S-BD Ref 116530
Breast Treatment Module SX EXF Package Ref 126850
ExaTilt Ref 171580
Mask TSRPO3-HNS set/10 Ref 363440
SSPS™ Cradle ExaFix™ Ref 111620
Mask MCN-6 set/10 Ref 119660
OmniBoard™ BTM-SX-S, MRC Ref 175060
Handgrips RE or TS, MRC, left Ref 111280L
Cranial AS for BBLX/TS, MRC, left Ref 122340L
Upper AS TS/MBLX PET-CT, set/2 Ref 122920
Mask DSPS™-FEVRONE, set/5 Ref 114780
EagleBoard™-2 M-Grip&Adaptor HS MR Ref 122890
H&N Baseplate Ref 110160
Rotatable Armrest Left LV Ref 122320L
MaxSupport™ S-A Ref 116300
Mask DSPS®-FSOSVRS, set/5 Ref 114420
Mask TUSSW3 set/10 Ref 377550
Mask DSPS®-FSOS, set/5 Ref 114520
Upper AS LV MRC, set/2 Ref 122710
Bolus Ref 153220
Profiles BreastBoardLX™, set/2 Ref 122360
Eamis lite™ system 123850 MRC Ref 123850
Mask TUSS set/10 Ref 376410
Mask LMPFC-5 set/10 Ref 139550
Mask TSRS3-HO set/10 Ref 369130
ExaFix Ref 111830L
Mask LMCFC-4 set/10 Ref 117540
Mask TSMP3-HNS set/10 Ref 363450
Mask DSPS®-FOSVRL, set/5 Ref 114460
Pelvic Plate Ref 133200
Profiles PelFix mask, set of 2 Ref 133210
ExaFix Ref 111730R
MaxSupport™ S-D MR Ref 116430
Mask REMCFC-5 set/10 Ref 357550
ExaTilt Ref 171500
DSPS-Prominent® SH profile set/2 Ref 113090
EagleBoard™-2 Adaptor OB EXF Ref 123020
Mask TSS-HNS, set/10 Ref 364410
DSPS® Cradle-I H Ref 112760
ExaFix Ref 111730L
Mask SSPS™-FSVRS set/10 Ref 115820
OmniBoard™ BTM-EX Ref 172130
Mask LMCFC-3P set/10 Ref 117535
Low Bridge Support MR Ref 120260
Block 1 CF Ref 110710
Handgrips RE or TS Ref 111230
Mask DSPS®-FSOSS, set/5 Ref 114320
Showing 351-400 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