Nipro Safelet Cath I - DRAP MDIR-0000382 (Class B)

DRAP REGISTERED MEDICAL DEVICE

Nipro Safelet Cath I is registered with DRAP under number MDIR-0000382 as a Class B (low to moderate risk) medical device, imported. The listed holder is Lab Link Enterprises. Its listed renewal date (21 May 2024) has passed, so ask the supplier for the renewal letter.

Screening result

i
Number type: imported, registered (Class B, C or D)
MDIR-0000382
✓
Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
!
Renewal date passed on 21 May 2024
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-00007
DeviceNipro Safelet Cath I
ClassB
Listed holderLab Link Enterprises
Holder addressM-203, Block 2, P.E.C.H.S Opp Ghousiya Masjid, Karachi., B-40, S.I.T.E, Karachi
Manufacturing siteM/s Nipro Corporation 3-9-3, Honjo-Nishi, Kita-Ku, Osaka-shi, Osaka, Japan
Issued22 May 2019
Renewal date21 May 2024
LicenceELI-00007

Specifications

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Screened 5 Oct 2026, 07:44 (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-0000076Nipro Syringe Without Needle [30ml, 50ml]Class A
MDIR-0001099Nipro Safelet Cath (IV Cannula ETFE Radiopaque catheter)Class B
MDIR-0001100Nipro Surefuser +Class C
MDIR-0001101Nipro Disposable Syringe (with needle)Class B
MDIR-0001102Nipro Infusion SetClass B
MDIR-0001103Nipro Wing Cath IV Cannula with Injection Port and Wing ETFE Radiopaque CatheterClass B
MDIR-0001104Nipro Syringe U-100 Insulin with Needle 1mlClass B
MDIR-0001605Nipro Spinal NeedleClass D
MDIR-0002076Amsino I.V. Administration Set [N-IS-01-A-ECEID]Class B
MDIR-0002645Infusion Set (IV Administration Set)Class B
MDIR-0002655Nipro Scalp Vein Set (PSV set) [19G, 20G, 21G, 22G, 23G, 24G, 25G, 27G]Class B
MDIR-0003202Nipro Safetouch Cath Winged (Safety IV Catheter) [14G, 16G, 18G, 20G, 22G, 24G]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.