STERIKING See-Through
Class A (low risk) · MDIE-0000106 · SBK International
DRAP ENLISTED MEDICAL DEVICE
STERIKING See-Through is enlisted with DRAP under number MDIE-0000106 as a Class A (low risk) medical device, imported. The listed holder is SBK International. Its listed renewal date (2 Sep 2025) has passed, so ask the supplier for the renewal letter.
Screening result
MDIE-0000106 · the class is taken from DRAP's list for this number
DRAP enlisted Class A list, 28 Aug 2025
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
ELI-00100
| Device | STERIKING See-Through |
|---|---|
| Class | A |
| Listed holder | SBK International |
| Holder address | 23, Valley Road, Street 3, Westridge 1, Rawalpindi, Godown: Same as above |
| Manufacturing site | M/s WIPAK OY WIPAKTIE 2, FI-15560 NASTOLA, FINLAND |
| Issued | 3 Sep 2020 |
| Renewal date | 2 Sep 2025 |
| Licence | ELI-00100 |
Specifications
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Screened 7 Oct 2026, 04:08 (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-0000107 | STERIKING Creps Papers | Class A |
| MDIE-0000108 | STERIKING PROWRAP | Class A |
| MDIE-0000343 | STERIKING LT BLUELINE POUCHES AND ROLLS Packaging Material (Pouches & Rolls) | Class A |
| MDIE-0000857 | MEDIBELL (Packing material Reels) | Class A |
| MDIE-0000858 | MEDIBELL (Medical crepe Paper) | Class A |
| MDIE-0000970 | MEDIBELL (Packing material Pouches) | Class A |
| MDIR-0004863 | VELSCOPE VX Oral Screening [83912, 4200, 5710, 5720] | Class B |
| MDIR-0007159 | MEDIBELL (IV Cannula with injection port) | Class B |
| MDIR-0007160 | MEDIBELL (IV Cannula with wings and heparin cap) | Class B |
| MDIR-0009186 | MEDIBELL Silicone Foley Catheter Urethral Catheter [2 Way] | Class B |
| MDIR-0009187 | MEDIBELL Latex Foley Catheter Urethral Catheter [2 Way] | Class B |
| MDIR-0009189 | Healthcare Lubricating Jelly | Class B |
Corrections
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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.