Rotapro Rotational Atherectomy System [Mechanical atherectomy system, coronary, line-powered] - DRAP MDIR-0004529 (Class D)

DRAP REGISTERED MEDICAL DEVICE

Rotapro Rotational Atherectomy System [Mechanical atherectomy system, coronary, line-powered] is registered with DRAP under number MDIR-0004529 as a Class D (high risk) medical device, imported. The listed holder is Ferozsons Laboratories Limited. It is listed as valid until 10 Jan 2028.

Screening result

i
Imported device, registered with DRAP as Class D (high risk)
MDIR-0004529 · 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 10 Jan 2028
✓
Holder has a DRAP import licence on file
ELI-00120
DeviceRotapro Rotational Atherectomy System [Mechanical atherectomy system, coronary, line-powered]
ClassD
Listed holderFerozsons Laboratories Limited
Holder addressGodown: Amangarh, Nowshera-KPK, Pakistan
Manufacturing siteM/s Boston Scientific Corporation 300, Boston Scientific Way, Marlborough MA 01752 M/s Boston Scientific Corporation 4100- Hamlin Ave N Saint Paul, MN USA 55112
Issued11 Jan 2023
Renewal date10 Jan 2028
LicenceELI-00120

Specifications

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Screened 5 Oct 2026, 15:55 (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.