DRAP REGISTERED MEDICAL DEVICE
Nipro Safetouch Cath (Safety IV Catheter) [14G, 16G, 18G, 20G, 22G, 24G] is registered with DRAP under number MDIR-0003203 as a Class B (low to moderate risk) medical device, imported. The listed holder is Lab Link Enterprises. It is listed as valid until 2 Feb 2027.
Screening result
MDIR-0003203 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00007
| Device | Nipro Safetouch Cath (Safety IV Catheter) [14G, 16G, 18G, 20G, 22G, 24G] |
|---|---|
| Class | B |
| Listed holder | Lab Link Enterprises |
| Holder address | M-203, Block 2, P.E.C.H.S Opp Ghousiya Masjid, Karachi. |
| Manufacturing site | M/s Nipro Corporation 3-9-3, Honjo-Nishi, Kita-ku, Osaka 531-8510, Japan M/s Nipro (Thailand) Corporation Limited., 10/2 Moo 8, Bangnomko, Sena, Phra Nakhon Si Ayutthaya 13110, Thailand |
| Issued | 3 Feb 2022 |
| Renewal date | 2 Feb 2027 |
| Licence | ELI-00007 |
Specifications
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Screened 5 Oct 2026, 18:39 (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-0000076 | Nipro Syringe Without Needle [30ml, 50ml] | Class A |
| MDIR-0000382 | Nipro Safelet Cath I | Class B |
| MDIR-0001099 | Nipro Safelet Cath (IV Cannula ETFE Radiopaque catheter) | Class B |
| MDIR-0001100 | Nipro Surefuser + | Class C |
| MDIR-0001101 | Nipro Disposable Syringe (with needle) | Class B |
| MDIR-0001102 | Nipro Infusion Set | Class B |
| MDIR-0001103 | Nipro Wing Cath IV Cannula with Injection Port and Wing ETFE Radiopaque Catheter | Class B |
| MDIR-0001104 | Nipro Syringe U-100 Insulin with Needle 1ml | Class B |
| MDIR-0001605 | Nipro Spinal Needle | Class D |
| MDIR-0002076 | Amsino I.V. Administration Set [N-IS-01-A-ECEID] | Class B |
| MDIR-0002645 | Infusion Set (IV Administration Set) | Class B |
| MDIR-0002655 | Nipro Scalp Vein Set (PSV set) [19G, 20G, 21G, 22G, 23G, 24G, 25G, 27G] | 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.