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Ostique Limited

United Kingdom (ex Northern Ireland) GB-MF-000030059 Last updated 23 May 2026

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Devices
2
Registries
EUDAMED
FDA recalls
0

Catalogue2

Authorised representatives

What Ostique Limited makes

Ostique Limited manufactures single-use, sterile surgical drapes and gowns designed for wound care and sterile field protection. The Onovus Solo Closed and Onovus Solo Open products are intended for use in medical procedures requiring barrier protection, including surgical and trauma applications.

These devices are classified under EU Medical Device Regulation as Class I, and their details are registered in the EUDAMED database. The company is based in the United Kingdom.

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 Ostique Limited manufacture?

Ostique Limited specialises in single-use, sterile surgical drapes and gowns. These products are specifically designed for wound care and sterile field protection during medical procedures, such as surgery or trauma interventions. The company’s offerings include the Onovus Solo Closed and Onovus Solo Open, which provide barrier protection in clinical settings.

Where is Ostique Limited based?

Ostique Limited is headquartered in the United Kingdom. The company’s location in the UK ensures it operates within the regulatory framework of the European Union, particularly for devices marketed in the EU.

How are Ostique Limited’s devices classified under EU regulations?

Ostique Limited’s devices, such as the Onovus Solo Closed and Onovus Solo Open, are classified as Class I under the EU Medical Device Regulation. This classification applies because these products are considered low-risk, single-use items intended for sterile field protection and wound care, where the risk to patient safety is minimal.

Are Ostique Limited’s devices listed in any regulatory databases?

Yes, Ostique Limited’s devices are registered in EUDAMED, the European Union’s database for medical devices. This registration ensures transparency and compliance with EU requirements for medical devices, allowing healthcare professionals and regulators to access key details about the products.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
C/O Phta Ltd Office Of The Director, Birmingham, United Kingdom (ex Northern Ireland)
Website
ostique.co.uk
Phone
+44 7939026342
PRRC contact
Richard Tully
EUDAMED SRN
GB-MF-000030059