DRAP REGISTERED MEDICAL DEVICE
BARD (Snare Retrieval Kit) [SRK35] is registered with DRAP under number MDIR-0005812 as a Class D (high risk) medical device, imported. The listed holder is Surgi World. It is listed as valid until 20 Nov 2028.
Screening result
MDIR-0005812 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00212
| Device | BARD (Snare Retrieval Kit) [SRK35] |
|---|---|
| Class | D |
| Listed holder | Surgi World |
| Holder address | 303, Muhammadia Plaza, College Road, Rawalpindi |
| Manufacturing site | M/s Bard Peripheral Vascular, Inc 1624 West 3rd Street Tempe, Arizona, 85281, U.S.A M/s Heraeus Medical Components, LLC 5030 Centerville Road St. Paul, MN 55127-2203, USA |
| Issued | 21 Nov 2023 |
| Renewal date | 20 Nov 2028 |
| Licence | ELI-00212 |
Specifications
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Screened 7 Oct 2026, 06:07 (Pakistan time). A screening aid, not an official DRAP verification.
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| MDIR-0001991 | Bard 3D Max Light Mesh [0117310, 0117311 0117312, 0117320 0117321, 0117322] | Class C |
| MDIR-0001997 | HICKMAN CENTRAL VENOUS CATHETER [0600310, 0600320, 0600570, 0600580, 0600600, 0600620] | Class D |
| MDIR-0001998 | BROVIAC Central Venous [0600520, 0600540, 0600040] | Class D |
Similar devices from other companies
Same device type listed by other holders, useful when comparing suppliers.
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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.