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
MDIR-0003691
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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
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Listed valid until 15 Aug 2027
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Holder has a DRAP import licence on file
ELI-00201
ELI-00201
| Device | Canack Single Kit Anesthesia Kit |
|---|---|
| Class | B |
| Listed holder | Freesia Enterprises |
| Holder address | 104, Dawn Plaza, Bank Road, Saddar, Rawalpindi. |
| Manufacturing site | M/s. Ningbo Luke Medical Devices Co., Ltd., Gujiayan Yangming Road 315400 Yuyao City, Zhejiang province China |
| Issued | 16 Aug 2022 |
| Renewal date | 15 Aug 2027 |
| Licence | ELI-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-0001961 | PROCARE Latex Examination Gloves Powdered Non-Sterile | Class A |
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| MDIR-0003334 | Canack Breathing filters [CK-01 Adult, CK-02 Pediatric, CK-02-01 Pediatric, CK-03-01 Adult, CK-04-01 Adult, CK-41 Adult, CK-11… | Class B |
| MDIR-0003687 | PROFEEL powder free latex surgical gloves sterile | Class B |
| MDIR-0003688 | COMFIT-NR Latex Surgical gloves powdered sterile | Class B |
| MDIR-0003689 | COMFIT PREMIUM-NR latex surgical gloves powdered sterile | Class B |
| MDIR-0003690 | PROFEEL double gloving system latex powder free latex surgical gloves sterile | Class B |
| MDIR-0003914 | Canack Endotracheal Tubes (Cuffed) | Class B |
| MDIR-0003915 | Canack Oropharyngeal Airways | Class B |
| MDIR-0003916 | Canack Wound Drainage System [Closed wound drainage system with drainage bag] | 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.
