Canack Single Kit Anesthesia Kit - DRAP MDIR-0003691 (Class B)

DRAP REGISTERED MEDICAL DEVICE

Canack Single Kit Anesthesia Kit is registered with DRAP under number MDIR-0003691 as a Class B (low to moderate risk) medical device, imported. The listed holder is Freesia Enterprises. It is listed as valid until 15 Aug 2027.

Screening result

i
Number type: imported, registered (Class B, C or D)
MDIR-0003691
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 15 Aug 2027
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Holder has a DRAP import licence on file
ELI-00201
DeviceCanack Single Kit Anesthesia Kit
ClassB
Listed holderFreesia Enterprises
Holder address104, Dawn Plaza, Bank Road, Saddar, Rawalpindi.
Manufacturing siteM/s. Ningbo Luke Medical Devices Co., Ltd., Gujiayan Yangming Road 315400 Yuyao City, Zhejiang province China
Issued16 Aug 2022
Renewal date15 Aug 2027
LicenceELI-00201

Specifications

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Screened 5 Oct 2026, 01:41 (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-0001961PROCARE Latex Examination Gloves Powdered Non-SterileClass A
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MDIR-0003687PROFEEL powder free latex surgical gloves sterileClass B
MDIR-0003688COMFIT-NR Latex Surgical gloves powdered sterileClass B
MDIR-0003689COMFIT PREMIUM-NR latex surgical gloves powdered sterileClass B
MDIR-0003690PROFEEL double gloving system latex powder free latex surgical gloves sterileClass B
MDIR-0003914Canack Endotracheal Tubes (Cuffed)Class B
MDIR-0003915Canack Oropharyngeal AirwaysClass B
MDIR-0003916Canack Wound Drainage System [Closed wound drainage system with drainage bag]Class 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.