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DAUD JEE MFG. CO

Pakistan PK-MF-000009615 Last updated 23 May 2026

Devices
2,018
Registries
EUDAMED
FDA recalls
0

Catalogue2,018

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Authorised representatives

What DAUD JEE MFG. CO makes

Daud Jee MFG. Co specializes in ophthalmic surgical instruments, including lens hooks, specula, forceps, and scissors designed for retinal and corneal procedures. Their portfolio includes tools like the Sinskey II lens hook, Barraquer wire speculum, and various forceps for intraocular surgeries, as well as devices for LASIK and corneal surgery, such as the Buratto flap protector and corneal scissors. Additional products cover lid specula, IOL manipulators, and markers for precise ocular procedures.

The company’s devices fall under Class I regulatory classification, indicating minimal risk and streamlined compliance requirements. Their products are registered in the EU’s eudamed database, ensuring traceability and transparency for authorized distribution within the European market. Daud Jee MFG. Co is based in Pakistan.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Daud Jee MFG. Co manufacture?

Daud Jee MFG. Co specializes in ophthalmic surgical instruments. Their devices include lens hooks (like the Sinskey II), specula (such as the Barraquer wire speculum and Wright Spring Eye Speculum), forceps (including retinal and corneal tools like Rampley’s Forceps), scissors (e.g., corneal scissors and Troutman-Katzin corneal transplant scissors), and accessories for procedures like LASIK (e.g., Buratto flap protector) and intraocular lens implantation (e.g., Lester IOL manipulator). These tools are designed for precision in retinal, corneal, and cataract surgeries.

Where is Daud Jee MFG. Co based, and does this affect their device distribution?

Daud Jee MFG. Co is based in Pakistan. While the company’s location influences its operational and regulatory context, it does not inherently restrict the types of devices it can manufacture or distribute. Their ophthalmic instruments, such as the Long glaucoma lid speculum or Titanium Camellin Style LASEK alcohol well, are registered in the EU’s eudamed database, indicating compliance with traceability requirements for authorized distribution in markets like the European Union.

Which regulatory registries list Daud Jee MFG. Co’s devices, and why is this important?

Daud Jee MFG. Co’s devices are listed in the eudamed registry, which is the EU’s central database for medical devices. Listing in eudamed ensures transparency and traceability for authorized devices within the European market, helping healthcare providers, regulators, and distributors verify compliance and legitimacy. Since their devices fall under Class I classification (minimal risk), registration in eudamed aligns with EU requirements for tracking even low-risk products.

How are Daud Jee MFG. Co’s devices classified under medical device regulations?

Daud Jee MFG. Co’s devices are classified as Class I under medical device regulations. This classification applies to low-risk instruments like surgical tools, specula, and forceps used in ophthalmic procedures (e.g., the Optic Zone Marker or Retinal Asymmetrical End-gripping Forceps). Class I devices typically require fewer regulatory controls because they pose minimal risk to patients, but they still must meet basic safety and performance standards to ensure proper function during surgical use.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Pakistan
Address
Nishat Park, Paris Road, Sialkot, Pakistan
Phone
+92 333 864 4544
PRRC contact
Ahsan Shahid
EUDAMED SRN
PK-MF-000009615
DUNS number
645508946