DRAP REGISTERED MEDICAL DEVICE
Bioteq Guide wire [BT-GW Series] is registered with DRAP under number MDIR-0007527 as a Class B (low to moderate risk) medical device, imported. The listed holder is Gulfam Brothers. It is listed as valid until 3 Nov 2029.
Screening result
i
Imported device, registered with DRAP as Class B (low to moderate risk)
MDIR-0007527 · the class is taken from DRAP's list for this number
MDIR-0007527 · 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
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 3 Nov 2029
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Holder has a DRAP import licence on file
ELI-00028
ELI-00028
| Device | Bioteq Guide wire [BT-GW Series] |
|---|---|
| Class | B |
| Listed holder | Gulfam Brothers |
| Holder address | Office No 702, 7th Floor, Land Mark Plaza, Jail Road, Lahore. |
| Manufacturing site | M/s Bioteque Corporation 5F-6, No. 23, Sec 1, Chang-An E. Road, Taipei 104, Taiwan. |
| Issued | 4 Nov 2024 |
| Renewal date | 3 Nov 2029 |
| Licence | ELI-00028 |
Specifications
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Screened 6 Oct 2026, 04:27 (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.
| MDIR-0007528 | Bioteq Drainage Catheter [BT-PD Series] | Class B |
| MDIR-0008710 | Bioteq Ureteral Stent Set Double J-type | Class C |
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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.