DRAP REGISTERED MEDICAL DEVICE
Cocoon PFO Occluder Accessory Set (PFO Occluder Delivery System) is registered with DRAP under number MDIR-0003770 as a Class D (high risk) medical device, imported. The listed holder is Easha Enterprises. It is listed as valid until 29 Sep 2027.
Screening result
MDIR-0003770
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00203
| Device | Cocoon PFO Occluder Accessory Set (PFO Occluder Delivery System) |
|---|---|
| Class | D |
| Listed holder | Easha Enterprises |
| Holder address | Office No.376, Khaleej Center, Saidpur Road, Near Rasheed Nursing Home, Rawalpindi |
| Manufacturing site | M/s Vascular Innovations Co., Ltd 88/38 Moo 1, 345 Rd., Bangtanai Pakkret, Nonthaburi-11120, Thailand |
| Issued | 30 Sep 2022 |
| Renewal date | 29 Sep 2027 |
| Licence | ELI-00203 |
Specifications
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Screened 5 Oct 2026, 07:42 (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.
| MDIR-0000503 | Cocoon Septal Occluder | Class D |
| MDIR-0000504 | COCOON PFO Occulder | Class D |
| MDIR-0000505 | Cocoon VSD Occluder | Class D |
| MDIR-0000506 | Cocoon Duct Occluder | Class D |
| MDIR-0003771 | Cocoon VSD Occluder Accessory Set II (VSD Occluder Delivery System) | Class D |
| MDIR-0003772 | Cocoon Duct Occluder Accessory Set (PDA Occluder Delivery System) | Class D |
| MDIR-0003773 | Cocoon Septal Occluder Accessory Set (ASD Occluder Delivery System) | Class D |
| MDIR-0007923 | Biomed CSF Flow Control Valve | Class D |
| MDIR-0008145 | Wacocel Layer Oxidized Regenerated Cellulose | Class D |
| MDIR-0008146 | Wacocel Standard Oxidized Regenerated Cellulose | Class D |
| MDIR-0008147 | Wacocel Knitting Oxidized Regenerated Cellulose | Class D |
| MDIR-0008148 | Wacocel Puffy Oxidized Regenerated Cellulose | Class D |
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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.
