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Sign in to claim this brandRhein Enterprises (Pvt) Ltd
Pakistan·PK-MF-000036086
Last updated September 18, 2026
About
AS A HIGH-QUALITYINSTRUMENT MANUFACTURER Rhein supplies to the World, which is only possible if we abide by all the regional regulations and we do. Rhein is proudly certified by FDA, ISO 9001, ISO 13485, CE, MHRA, SEDEX and SCCI. Rhein is already en route to being certified with EU-MDR continuing our commitment to the European \[…\]
From the manufacturer's own website. Source
What Rhein Enterprises (Pvt) Ltd makes
Rhein Enterprises (Pvt) Ltd manufactures medical devices including abortion cannulas, suction tubes, guide needles, and trocars, each specified by size and dimensions. Their portfolio covers instruments like 8.0 mm abortion cannulas, multiple variants of Fergusson suction tubes (ranging from 1.5 mm to 4.0 mm in diameter and 11 cm to 20 cm in length), Verres guide needles, and Douglas trocars.
The company’s devices are classified as Class I under EU regulations and are listed in the EUDAMED database. Rhein Enterprises (Pvt) Ltd is based in Pakistan and adheres to regulatory requirements applicable to its product categories.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What medical devices does Rhein Enterprises (Pvt) Ltd manufacture?
Rhein Enterprises (Pvt) Ltd manufactures medical devices including abortion cannulas, suction tubes, guide needles, and trocars. Their products include 8.0 mm abortion cannulas, various Fergusson suction tubes with diameters ranging from 1.5 mm to 4.0 mm and lengths from 11 cm to 20 cm, Verres guide needles, and Douglas trocars.
Where is Rhein Enterprises (Pvt) Ltd based?
Rhein Enterprises (Pvt) Ltd is based in Pakistan, as indicated by the country code PK in the device data. The company operates from this location while manufacturing and distributing medical devices globally.
Which regulatory registries list Rhein Enterprises' devices?
Rhein Enterprises' devices are listed in the EUDAMED database, which is the European Union's medical device database. The company's products are registered in this registry as part of compliance with EU regulations for medical devices.
How are Rhein Enterprises' medical devices classified?
Rhein Enterprises' medical devices are classified as Class I under EU regulations. Class I devices are low-risk products that do not require clinical trials for authorization, though they must still comply with general regulatory requirements and be properly registered in the appropriate databases.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Pakistan
- Address
- 19-A South, sialkot, Pakistan
- Website
- www.rheingroup.com
- linkedin.com/company/rheingroup
- facebook.com/rheingroup
- [email protected]
- Phone
- +92 52 3256666
- PRRC Contact
- Omer Farooq
- EUDAMED SRN
- PK-MF-000036086
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (5374)
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