Capoiox FX Extra-corporeal Membrane Oxygenator - DRAP MDIR-0004371 (Class D)

DRAP REGISTERED MEDICAL DEVICE

Capoiox FX Extra-corporeal Membrane Oxygenator is registered with DRAP under number MDIR-0004371 as a Class D (high risk) medical device, imported. The listed holder is Universal Enterprises. It is listed as valid until 21 Dec 2027.

Screening result

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Imported device, registered with DRAP as Class D (high risk)
MDIR-0004371 · the class is taken from DRAP's list for this number
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 21 Dec 2027
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Holder has a DRAP import licence on file
ELI-00079
DeviceCapoiox FX Extra-corporeal Membrane Oxygenator
ClassD
Listed holderUniversal Enterprises
Holder address29, Block-3, Overseas Co-Operative Housing Society, Stadium Road, Karachi
Manufacturing siteM/s Terumo Corporation, 44-1, 2-Chome, Hatagaya, Shibuyaku, Tokyo, Japan M/s Ashitaka Factory of Terumo Corporation, 150 Maimaigi-cho, Fujinomia City Shizuoka Prefacture Japan
Issued22 Dec 2022
Renewal date21 Dec 2027
LicenceELI-00079

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Screened 6 Oct 2026, 12:58 (Pakistan time). A screening aid, not an official DRAP verification.

More devices from this holder

Other DRAP registrations and enlistments listed for the same company.

MDIR-0002552Capiox Oxygenator [3CX*RX15RW30 3CX*RX15RE30 3CX*RX15RW40 3CX*RX15RE40]Class D
MDIR-0003405Carbon Sterile Surgical BladesClass B
MDIR-0005692Terumo Custom Tubing PackClass B
MDIR-0005743Capiox NX19 Oxygenator with Integrated Arterial Filter and UltraPrime TechnologyClass B
MDIR-0006940AQUABIRD Surgical Sealant. [MAB2G-01, MAB1G-01]Class D

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Source: DRAP's published provisional lists. A screening aid, not an official DRAP verification; confirm with DRAP and the supplier's original documents.