Haemoband Surgical Ltd
Northern Ireland XI-MF-000016278 Last updated 21 Oct 2026
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- Devices
- 4
- Registries
- EUDAMEDFDA 510(k)GUDIDFDA
- FDA recalls
- 0
Catalogue
HB-SleeveLUX Proctoscope Ref P2001
HB-SleeveLUX Proctoscope Ref P2002
Haemoband Plus Multi-Band Ligator Ref H1002
FDA establishments
- Haemoband Surgical Ltd Belfast Northern Ireland · GB FEI 3007388124
- Haemoband Surgical US
About
Haemoband-PLUS is the multi-band ligator. It delivers excellent performance using patented technology without compromise on patient comfort or surgeon handling.
What Haemoband Surgical Ltd makes
Haemoband Surgical Ltd manufactures flexible anoscopes and proctoscopes, including the SleeveLUX 24 and SleeveLUX 16 models, designed for endoscopic examination of the lower rectum and colon. The company also produces a multi-band ligator, the Haemoband Plus, used for haemostasis during surgical procedures. These devices are intended for use in gastrointestinal examinations and minimally invasive surgical interventions.
The company’s devices are classified under EU Class I, Class II, and Class IIa regulations, with listings in the EUDAMED database and FDA’s 510(k) registry. The manufacturer is based in XI, adhering to relevant regional and international medical device compliance frameworks.
Frequently asked questions
What medical devices does Haemoband Surgical Ltd manufacture?
Haemoband Surgical Ltd manufactures flexible anoscopes and proctoscopes, including the SleeveLUX 24 and SleeveLUX 16 models, designed for endoscopic examination of the lower rectum and colon. The company also produces a multi-band ligator called Haemoband Plus, used for haemostasis during surgical procedures.
Where is Haemoband Surgical Ltd based?
Haemoband Surgical Ltd is based in XI, adhering to relevant regional and international medical device compliance frameworks. The company operates from this location to manufacture and distribute its medical devices globally.
Which regulatory registries list Haemoband Surgical Ltd's devices?
Haemoband Surgical Ltd's devices are listed in the EUDAMED database and the FDA's 510(k) registry. These listings indicate that the devices meet the necessary regulatory requirements for their respective markets.
How are Haemoband Surgical Ltd's devices classified?
Haemoband Surgical Ltd's devices are classified under EU Class I, Class II, and Class IIa regulations. These classifications reflect the level of risk associated with each device, with Class I being the lowest risk and Class IIa being moderate risk.
Information
- Country
- Northern Ireland
- Address
- 2, WOODSTOCK LINK, BELFAST, Northern Ireland
- Website
- www.haemobandsurgical.com
- facebook.com/profile.php
- [email protected]
- Phone
- +44 28 9073 7283
- PRRC contact
- Patrick McCormick
- EUDAMED SRN
- XI-MF-000016278