ABLE - DRAP MDIR-0001075 (Class B)

DRAP REGISTERED MEDICAL DEVICE

ABLE (Disposable Blood Lines) is registered with DRAP under number MDIR-0001075 as a Class B (low to moderate risk) medical device, imported. The listed holder is Flowtronix Systems. Its listed renewal date (12 Dec 2024) has passed, so ask the supplier for the renewal letter.

Screening result

i
Imported device, registered with DRAP as Class B (low to moderate risk)
MDIR-0001075 · the class is taken from DRAP's list for this number
✓
Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
!
Renewal date passed on 12 Dec 2024
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
i
Holder not found in DRAP's published licence list
That list covers manually issued licences only. Ask for a copy of the establishment licence.
DeviceABLE (Disposable Blood Lines)
ClassB
Listed holderFlowtronix Systems
Holder addressFlat No. 02, 1st Floor Al-Ashraf Plaza, Range Road, Rawalpindi
Manufacturing siteM/s. Guangdon Baihe Medical Technology Co., Ltd No. 89, Taoyuan East Road, Nanhai, Foshan 528225, Guangdong Province, China
Issued13 Dec 2019
Renewal date12 Dec 2024

Specifications

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Screened 5 Oct 2026, 17:36 (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.

MDIE-0002001Hemonart Compact One 9 ACT AnalyzerClass A
MDIR-0001065ABLE (Disposable Fistula Needles)Class B
MDIR-0001066ABLE (Disposable Haemodialysers)Class C
MDIR-0001067ABLE (Central Venous Catheter Kit).Class D
MDIR-0001068ANDOCOR Cardiopleagia SetsClass D
MDIR-0001069ANDOCOR Pericardial SumpClass B
MDIR-0001070ANDOCOR Ostial Perfusion CannulaeClass D
MDIR-0001071ANDOCOR Silicone Vent CatheterClass D
MDIR-0001072ANDOCOR (Vessel Cannula with closed back check valve)Class B
MDIR-0001073ANDOCOR Cannulation Torniquet SetClass B
MDIR-0001074IBC Aortic PunchClass B
MDIR-0001076ABLE (Disposable Pressure Transducers)Class B

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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.