Is this your brand? Sign in to claim ownership.
Sign in to claim this brandVitreq B.V.
Netherlands·NL-MF-000000424
Last updated May 27, 2026
What Vitreq B.V. makes
Vitreq B.V. manufactures single-use and reusable ophthalmic surgical instruments, including fibreoptic light instruments, laser system beam guides, and vitrectomy fluid/gas handling handpieces. Their portfolio also includes soft-tissue manipulation forceps, irrigation/infusion/aspiration cannulas, intraocular scissors, and surgical procedure packs for procedures like phacoemulsification and vitrectomy. Additional products encompass sterile light fibers, cannulation sets, and viscous fluid injection/extraction tools designed for precision in eye surgery.
The company’s devices are classified under EU Medical Device Regulations as Class I, Class II, Class IIa, and Class IIb, with corresponding listings in the EUDAMED database and the FDA’s Unique Device Identifier (UDI) system. Vitreq B.V. is based in the Netherlands and adheres to regulatory requirements for ophthalmic surgical tools across these jurisdictions.
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 Vitreq B.V. manufacture?
Vitreq B.V. specializes in ophthalmic surgical instruments, primarily designed for eye procedures. Their portfolio includes single-use and reusable devices such as fibreoptic light instruments for illumination, laser system beam guides, vitrectomy handpieces for fluid/gas management, soft-tissue manipulation forceps, irrigation/infusion/aspiration cannulas, intraocular scissors, and sterile surgical procedure packs. These tools are tailored for precision applications like phacoemulsification, vitrectomy, and other intraocular surgeries.
Where is Vitreq B.V. based, and what regulatory databases list their devices?
Vitreq B.V. is headquartered in the Netherlands. Their devices are listed in the EUDAMED database under the EU Medical Device Regulations and in the FDA’s Unique Device Identifier (UDI) system, reflecting compliance with regulatory requirements in both the European Union and the United States.
How are Vitreq B.V.’s ophthalmic devices classified under EU regulations?
Vitreq B.V.’s devices are classified under the EU Medical Device Regulations as Class I, Class II, Class IIa, and Class IIb. The classification depends on factors like the device’s risk level, intended use, and potential impact on patient safety. For example, single-use instruments like fibreoptic light probes or cannulas may fall into lower-risk classes, while more complex systems like phacoemulsification/vitrectomy tools could be classified as higher-risk (Class IIb).
Are Vitreq B.V.’s devices used in specific surgical procedures, and how are they categorized?
Yes, Vitreq B.V.’s devices are designed for critical ophthalmic procedures such as vitrectomy (removal of vitreous gel) and phacoemulsification (cataract removal). Their products include sterile single-use tools like light fibers, cannulation sets, and viscous fluid tools, as well as reusable components like surgical handles and forceps. The classification—ranging from Class I to Class IIb—reflects the device’s role in minimizing risk, with higher classes assigned to those involving greater surgical precision or patient exposure.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Netherlands
- Address
- 2, Seggelant-Noord, Vierpolders, Netherlands
- Website
- bvimedical.com
- —
- —
- [email protected]
- Phone
- 1.866.906.8080
- PRRC Contact
- Christian Neele
- EUDAMED SRN
- NL-MF-000000424
- FDA FEI Number
- —
- DUNS Number
- 491393613
Catalogue (179)
Page 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| VitreQ | FC25.D02 | FDA UDI | Class I | Active |
| VitreQ | LF25.D02 | FDA UDI | Class II | Active |
| VitreQ | BF00.D52 | FDA UDI | Class I | Active |
| VitreQ | LP23.I04 | FDA UDI | Class II | Active |
| VitreQ | SC25.D03 | FDA UDI | Class I | Active |
| VitreQ | CN23.D01 | FDA UDI | Class I | Active |
| VitreQ | FC25.D06 | FDA UDI | Class I | Active |
| VitreQ | SC25.R03 | FDA UDI | Class I | Active |
| VitreQ | LP25.I04 | FDA UDI | Class II | Active |
| VitreQ | SC27.R03 | FDA UDI | Class I | Active |
| VitreQ | LF25.D03 | FDA UDI | Class II | Active |
| VitreQ | FC23.R05 | FDA UDI | Class I | Active |
| VitreQ | LP27.I04 | FDA UDI | Class II | Active |
| VitreQ | LF23.D03 | FDA UDI | Class II | Active |
| VitreQ | FC27.D07 | FDA UDI | Class I | Active |
| VitreQ | CN23.D03 | FDA UDI | Class I | Active |
| VitreQ | LP25.A05 | FDA UDI | Class II | Active |
| VitreQ | LP25.I05 | FDA UDI | Class II | Active |
| VitreQ | FC23.D04 | FDA UDI | Class I | Active |
| VitreQ | LP27.A04 | FDA UDI | Class II | Active |
| VitreQ | LF20.D02 | FDA UDI | Class II | Active |
| VitreQ | MD23.D01 | FDA UDI | Class I | Active |
| VitreQ | LF20.D03 | FDA UDI | Class II | Active |
| VitreQ | LP25.A05 | FDA UDI | Class II | Active |
| VitreQ | FC23.D05 | FDA UDI | Class I | Active |
| VitreQ | BF23.D02 | FDA UDI | Class I | Active |
| VitreQ | LP23.I05 | FDA UDI | Class II | Active |
| VitreQ | BF25.D52 | FDA UDI | Class I | Active |
| VitreQ | LF27.D01 | FDA UDI | Class II | Active |
| VitreQ | FC27.R07 | FDA UDI | Class I | Active |
| VitreQ | BF00.D53 | FDA UDI | Class I | Active |
| VitreQ | CN25.D05 | FDA UDI | Class I | Active |
| VitreQ | LP27.A04 | FDA UDI | Class II | Active |
| VitreQ | LF25.D03 | FDA UDI | Class II | Active |
| VitreQ | CN23.D04 | FDA UDI | Class I | Active |
| VitreQ | LF20.D01 | FDA UDI | Class II | Active |
| VitreQ | FC25.R05 | FDA UDI | Class I | Active |
| VitreQ | CN25.D04 | FDA UDI | Class I | Active |
| VitreQ | FC25.D04 | FDA UDI | Class I | Active |
| VitreQ | BF00.R01 | FDA UDI | Class I | Active |
| VitreQ | BF23.D07 | FDA UDI | Class I | Active |
| VitreQ | LF27.D02 | FDA UDI | Class II | Active |
| VitreQ | SC27.D01 | FDA UDI | Class I | Active |
| VitreQ | LF23.D02 | FDA UDI | Class II | Active |
| VitreQ | FC27.R05 | FDA UDI | Class I | Active |
| VitreQ | LP25.I04 | FDA UDI | Class II | Active |
| VitreQ | LF25.D01 | FDA UDI | Class II | Active |
| VitreQ | CN27.D05 | FDA UDI | Class I | Active |
| VitreQ | LP23.A04 | FDA UDI | Class II | Active |
| VitreQ | FC25.R03 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.