DCH AURIGA (M) SDN BHD
MalaysiaActiveGDPMD certified
License MDA-5872-WDP124 · valid through Apr 28, 2027
Registered products
48
48 imported · 0 domestic
Principal brands
0
No brands recorded
Decision-makers
—
Coming soon
Confidence
4/5
Verified Jun 2, 2026
About DCH AURIGA (M) SDN BHD
DCH AURIGA (M) SDN BHD and operates under a Malaysia medical device distribution license (MDA-5872-WDP124). They hold registrations for 48 products across the national device registry.
Address: LOT 6, PERSIARAN PERUSAHAAN, SEKSYEN 23, SHAH ALAM,
Recent product registrations
Showing 10 of 48| Product | Manufacturer | Type | Risk |
|---|---|---|---|
AMDS HYBRID PROSTHESIS GD9315321-62118 | AMDS HYBRID PROSTHESIS | MMDR_GENERAL_D | D |
ARTIVION™ TUVA™ BX PERIPHERAL BALLOON EXPANDABLE PTFE COVERED STENT SYSTEM GD5969026-227669 | ARTIVION™ TUVA™ BX | MMDR_GENERAL_D | D |
E-VITA OPEN NEO GD8330420-50236 | JOTEC | MMDR_GENERAL_D | D |
FLOWNIT BIOSEAL AND FLOWWEAVE BIOSEAL GD6138820-49551 | JOTEC | MMDR_GENERAL_D | D |
E-NSIDE TAAA MULTIBRANCH STENT GRAFT SYSTEM GD6250320-49019 | JOTEC | MMDR_GENERAL_D | D |
E-LIAC STENT GRAFT SYSTEM GD6813620-47854 | JOTEC | MMDR_GENERAL_D | D |
E-XPAND STENT GRAFT BALLOON CATHETER GD2422920-47256 | JOTEC | MMDR_GENERAL_D | D |
E-WIRE GUIDE WIRE GB4299220-46732 | JOTEC | MMDR_GENERAL_B | B |
GUIDEWIRE SFC-400/6-018/NITI-PT 400 CM, 0.018'' GD6460025-205134 | 46011984 | MMDR_GENERAL_D | D |
FLOWLINE BIPORE EPTFE VASCULAR GRAFT GC4236225-201881 | JOTEC | MMDR_GENERAL_C | C |
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