HILBRO INTERNATIONAL (PVT) LIMITED
Pakistan PK-MF-000025041 Last updated 25 Oct 2026
- Devices
- 3,164
- Registries
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
Hilbro Ref 08.0113.20
Hilbro Ref 28.1492.06
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Hilbro Ref 14.0294.14
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Hilbro Ref 10.0544.13
Hilbro Ref 14.0353.19
Hilbro Ref 14.0292.14
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Hilbro Ref 10.0059.28
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Hilbro Ref 10.0024.13
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Hilbro Ref 14.0151.18
Hilbro Ref 12.0110.16
Hilbro Ref 10.0165.09
Hilbro Ref 10.5361.28
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Hilbro Ref 10.0520.22
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Hilbro Ref 10.5636.27
Hilbro Ref 12.0356.25
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Hilbro Ref 14.0116.14
Hilbro Ref 06.0194.08
Hilbro Ref 28.0340.03
Hilbro Ref 12.9116.14
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What HILBRO INTERNATIONAL (PVT) LIMITED makes
Hilbro International (Pvt) Limited manufactures Magill Catheter Introducing Forceps in two lengths: 17cm and 15cm. These devices are designed for medical procedures requiring the insertion of catheters, such as endotracheal intubation.
The Magill Catheter Introducing Forceps are classified as Class I medical devices and are listed in the EU’s eudamed registry. The company is based in Pakistan.
Frequently asked questions
What types of medical devices does Hilbro International (Pvt) Limited manufacture?
Hilbro International (Pvt) Limited specializes in manufacturing Magill Catheter Introducing Forceps, which come in two lengths: 15cm and 17cm. These devices are specifically designed to assist in medical procedures like endotracheal intubation, where catheters need to be inserted into the body.
Where is Hilbro International (Pvt) Limited based?
The company is headquartered in Pakistan, as indicated in its regulatory documentation.
Which regulatory registries list Hilbro International (Pvt) Limited’s devices?
The Magill Catheter Introducing Forceps manufactured by Hilbro International (Pvt) Limited are listed in the eudamed registry, which is the European database for medical devices. This registry tracks devices authorized for use within the EU.
How are Hilbro International (Pvt) Limited’s devices classified?
The Magill Catheter Introducing Forceps produced by Hilbro International (Pvt) Limited fall under Class I medical device classification. This classification is typically assigned to low-risk devices that pose minimal risk to patients, such as certain surgical instruments or basic diagnostic tools.
Information
- Country
- Pakistan
- Address
- Hilbro Industrial Park, 12 Km, , Sialkot, Pakistan
- [email protected]
- Phone
- +92 52 330 8101 03
- PRRC contact
- Tariq Safder
- EUDAMED SRN
- PK-MF-000025041
- FDA FEI number
- 3003431869