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Medical Device Division · registration 210120Cancelled

Elixir Medical

Hong KongAdapter/Connectors, Angioplasty Balloon Dilatation CatheterClass IVElixir Medical Corporation
Official record identity
MDACS listing number
210120
Model name
XPANSE Balloon Dilatation Catheter (DCR1508, DCR1509, DCR1510, DCR1511, DCR1512, DCR1513, DCR1514, DCR1515, DCR1516, DCR1517, DCR1518, DCR1519, DCR1520, DCR1521, DCR1522, DCR1523, DCR1524, DCR1525, DCR1526, DCR1527, DCR1528, DCR1529, DCR1530, DCR1531, DCR1532, DCR1533, DCR1534, DCR1535, DCR1536, DCR1537, DCR1538, DCR1539, DCR1540, DCR2008, DCR2009, DCR2010, DCR2011, DCR2012, DCR2013, DCR2014, DCR2015, DCR2016, DCR2017, DCR2018, DCR2019, DCR2020, DCR2021, DCR2022, DCR2023, DCR2024, DCR2025, DCR2026, DCR2027, DCR2028, DCR2029, DCR2030, DCR2031, DCR2032, DCR2033, DCR2034, DCR2035, DCR2036, DCR2037, DCR2038, DCR2039, DCR2040, DCR2208, DCR2209, DCR2210, DCR2211, DCR2212, DCR2213, DCR2214, DCR2215, DCR2216, DCR2217, DCR2218, DCR2219, DCR2220, DCR2221, DCR2222, DCR2223, DCR2224, DCR2225, DCR2226, DCR2227, DCR2228, DCR2229, DCR2230, DCR2231, DCR2232, DCR2233, DCR2234, DCR2235, DCR2236, DCR2237, DCR2238, DCR2239, DCR2240, DCR2508, DCR2509, DCR2510, DCR2511, DCR2512, DCR2513, DCR2514, DCR2515, DCR2516, DCR2517, DCR2518, DCR2519, DCR2520, DCR2521, DCR2522, DCR2523, DCR2524, DCR2525, DCR2526, DCR2527, DCR2528, DCR2529, DCR2530, DCR2531, DCR2532, DCR2533, DCR2534, DCR2535, DCR2536, DCR2537, DCR2538, DCR2539, DCR2540, DCR2708, DCR2709, DCR2710, DCR2711, DCR2712, DCR2713, DCR2714, DCR2715, DCR2716, DCR2717, DCR2718, DCR2719, DCR2720, DCR2721, DCR2722, DCR2723, DCR2724, DCR2725, DCR2726, DCR2727, DCR2728, DCR2729, DCR2730, DCR2731, DCR2732, DCR2733, DCR2734, DCR2735, DCR2736, DCR2737, DCR2738, DCR2739, DCR2740, DCR3008, DCR3009, DCR3010, DCR3011, DCR3012, DCR3013, DCR3014, DCR3015, DCR3016, DCR3017, DCR3018, DCR3019, DCR3020, DCR3021, DCR3022, DCR3023, DCR3024, DCR3025, DCR3026, DCR3027, DCR3028, DCR3029, DCR3030, DCR3031, DCR3032, DCR3033, DCR3034, DCR3035, DCR3036, DCR3037, DCR3038, DCR3039, DCR3040, DCR3208, DCR3209, DCR3210, DCR3211, DCR3212, DCR3213, DCR3214, DCR3215, DCR3216, DCR3217, DCR3218, DCR3219, DCR3220, DCR3221, DCR3222, DCR3223, DCR3224, DCR3225, DCR3226, DCR3227, DCR3228, DCR3229, DCR3230, DCR3231, DCR3232, DCR3233, DCR3234, DCR3235, DCR3236, DCR3237, DCR3238, DCR3239, DCR3240, DCR3508, DCR3509, DCR3510, DCR3511, DCR3512, DCR3513, DCR3514, DCR3515, DCR3516, DCR3517, DCR3518, DCR3519, DCR3520, DCR3521, DCR3522, DCR3523, DCR3524, DCR3525, DCR3526, DCR3527, DCR3528, DCR3529, DCR3530, DCR3531, DCR3532, DCR3533, DCR3534, DCR3535, DCR3536, DCR3537, DCR3538, DCR3539, DCR3540, DCR3708, DCR3709, DCR3710, DCR3711, DCR3712, DCR3713, DCR3714, DCR3715, DCR3716, DCR3717, DCR3718, DCR3719, DCR3720, DCR3721, DCR3722, DCR3723, DCR3724, DCR3725, DCR3726, DCR3727, DCR3728, DCR3729, DCR3730, DCR3731, DCR3732, DCR3733, DCR3734, DCR3735, DCR3736, DCR3737, DCR3738, DCR3739, DCR3740, DCR4008, DCR4009, DCR4010, DCR4011, DCR4012, DCR4013, DCR4014, DCR4015, DCR4016, DCR4017, DCR4018, DCR4019, DCR4020, DCR4021, DCR4022, DCR4023, DCR4024, DCR4025, DCR4026, DCR4027, DCR4028, DCR4029, DCR4030, DCR4031, DCR4032, DCR4033, DCR4034, DCR4035, DCR4036, DCR4037, DCR4038, DCR4039, DCR4040, DCR4508, DCR4509, DCR4510, DCR4511, DCR4512, DCR4513, DCR4514, DCR4515, DCR4516, DCR4517, DCR4518, DCR4519, DCR4520, DCR4521, DCR4522, DCR4523, DCR4524, DCR4525, DCR4526, DCR4527, DCR4528, DCR4529, DCR4530, DCR4531, DCR4532, DCR4533, DCR4534, DCR4535, DCR4536, DCR4537, DCR4538, DCR4539, DCR4540)
Registration date
April 09, 2021
Source update date
June 13, 2025
Status
Cancelled
Official value: Delisted
Classification
Risk class
Class IV
Official value: IV
Published category
Adapter/Connectors, Angioplasty Balloon Dilatation Catheter
Published parties
Registrant / registration holder
Emergo Hong Kong Limited
Official description

Adapter/Connectors, Angioplasty Balloon Dilatation Catheter

Additional source fields
AMD nomenclature code
17787
Traditional Chinese local responsible person
埃默高香港有限公司
Local responsible person phone
22769196
Published manufacturer address
920 N McCarthy Blvd., Suite 100, Milpitas, CA 95035, USA
Published remarks
Delisted.
Delist date
2025-06-13
About this record

This page mirrors one official MDACS listing. Roman-numeral classes use Hong Kong’s general medical-device scheme, while letter classes use the IVD scheme. Valid, expired, and delisted records remain distinguishable; no mixed classification scale is fabricated.