DRAP registered medical device · imported
Ankaferd Blood Stopper
Class D (high risk) · MDIR-0003837 · Neutro Health Care
✓ DRAP status
Listed
Valid until 16 Oct 2027
Screened against DRAP's published lists
DRAP REGISTERED MEDICAL DEVICE
Ankaferd Blood Stopper (Wet Tampon gauze Pad) is registered with DRAP under number MDIR-0003837 as a Class D (high risk) medical device, imported. The listed holder is Neutro Health Care. It is listed as valid until 16 Oct 2027.
Screening result
i
Imported device, registered with DRAP as Class D (high risk)
MDIR-0003837 · the class is taken from DRAP's list for this number
MDIR-0003837 · the class is taken from DRAP's list for this number
✓
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
✓
Listed valid until 16 Oct 2027
i
Holder not found in DRAP's published licence list
That list covers manually issued licences only. Ask for a copy of the establishment licence.
That list covers manually issued licences only. Ask for a copy of the establishment licence.
| Device | Ankaferd Blood Stopper (Wet Tampon gauze Pad) |
|---|---|
| Class | D |
| Listed holder | Neutro Health Care |
| Holder address | 22-M, Gulberg-III, Lahore. |
| Manufacturing site | M/s. BikarIlac San. ve Tic. Ltd. sti. GullubaglarMah. Ankara Cad. SirinSokak No: 14 Pendik / ISTANBUL / TURKEY. |
| Issued | 17 Oct 2022 |
| Renewal date | 16 Oct 2027 |
Specifications
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Screened 7 Oct 2026, 00:04 (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.