Circumplast Circumcision Device - DRAP MDIR-0008787 (Class B)

DRAP REGISTERED MEDICAL DEVICE

Circumplast Circumcision Device is registered with DRAP under number MDIR-0008787 as a Class B (low to moderate risk) medical device, imported. The listed holder is Sanyoh international. It is listed as valid until 6 Apr 2030.

Screening result

i
Imported device, registered with DRAP as Class B (low to moderate risk)
MDIR-0008787 · 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
✓
Listed valid until 6 Apr 2030
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.
DeviceCircumplast Circumcision Device
ClassB
Listed holderSanyoh international
Holder addressOffice# 2, Flat #8. Block 19. Allah Dad Plaza, G-8 Markaz. Islamabad
Manufacturing siteM/s Emboss Medical Limited 128 City Road, London, EC1V 2NX, United Kingdom
Issued7 Apr 2025
Renewal date6 Apr 2030

Specifications

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Screened 6 Oct 2026, 17:06 (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-0001616XINWELL Clip AppliersClass A
MDIR-0008846XINWEL Disposable Ligation Clips (Homopolyformaldehy de)Class B
MDIR-0008847XINWELL Disposable TrocarClass B
MDIR-0008848XINWELL Disposable Core Biopsy InstrumentClass 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.