KLF Infusion Set for Single Use
Class B (low to moderate risk) · MDIR-0008610 · Ali Gohar & Company (Private) Limited.
DRAP REGISTERED MEDICAL DEVICE
KLF Infusion Set for Single Use is registered with DRAP under number MDIR-0008610 as a Class B (low to moderate risk) medical device, imported. The listed holder is Ali Gohar & Company (Private) Limited.. It is listed as valid until 27 Mar 2030.
Screening result
MDIR-0008610 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00004
| Device | KLF Infusion Set for Single Use |
|---|---|
| Class | B |
| Listed holder | Ali Gohar & Company (Private) Limited. |
| Holder address | State Life Building I-B, I.I Chundrigar Road, Karachi. |
| Manufacturing site | M/s Wenzhou K.L.F. Medical Plastics Co., Ltd. No 29, Gangqiang Road, Airport New Area, Yongxing Street Longwan District, 325000 Wenzhou, Zhejiang Peoples Republic of China. |
| Issued | 28 Mar 2025 |
| Renewal date | 27 Mar 2030 |
| Licence | ELI-00004 |
Specifications
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Screened 7 Oct 2026, 02:52 (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.