BD Venflon TM Pro IV Cannulas - DRAP MDIR-0000034 (Class B)

DRAP REGISTERED MEDICAL DEVICE

BD Venflon TM Pro IV Cannulas (G16, G18, G20 & G22) is registered with DRAP under number MDIR-0000034 as a Class B (low to moderate risk) medical device, imported. The listed holder is Asto Life Sciences (Pvt) Ltd. Its listed renewal date (4 Jul 2022) 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-0000034 · 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
!
Renewal date passed on 4 Jul 2022
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
✓
Holder has a DRAP import licence on file
ELI-00103
DeviceBD Venflon TM Pro IV Cannulas (G16, G18, G20 & G22)
ClassB
Listed holderAsto Life Sciences (Pvt) Ltd
Holder address44/1.Block -K, Model Town Lahore
Manufacturing siteManufacturer: M/s Becton Dickinson Infusion Therapy AB Florettgatan 29C, PO Box 631, SE, 251 06, Helsingborg, Sweden Manufacturing Site: M/s Becton Dickinson Medical (S) Pte Ltd.,30 Taus Avenue-2, 639461 Singapore
Issued6 Dec 2018
Renewal date4 Jul 2022
LicenceELI-00103

Specifications

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Screened 6 Oct 2026, 18:37 (Pakistan time). A screening aid, not an official DRAP verification.

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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.