EU → North America Device Access

BNOS MediTECH

GB-MF-000008883 · United Kingdom · Halstead, Essex,

BNOS MediTECH is registered in the European database on medical devices as a manufacturer, with 601 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIb318
Class IIa283

Most frequent device types declared: BS PROBE-BS SCHRADER HOSE, OXYGEN, MA4, TE, Pin Index, Therapy, 2 x BS Schrader, 0-15 LPM, MA4, TE, Pin Index, Therapy, 2 x BS Schrader, 0-25 LPM, Oxygen Regulator, Bullnose (Benelux), 1 x AFNOR NF S90-116:1988, Thera, Oxygen Regulator, Pin Index (Articulating Yoke), 1 x DIN 13260-2:2004 .

Among these devices, 3 are declared sterile, 599 active.

Authorised representative in the Union: Medical Device Management Ltd.

Devices declared under this manufacturer

Showing 12 of 601 declared devices.

Catalogue references include 151-0002-00, 670-0583-00, 673-0555-00, 679-0004-10\t, 779-0205-12\t, 781-0062-00.

European nomenclature codes declared: A030104, Z12030103, R9080, R028001, Z12030104.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED601
Country of registrationUnited Kingdom

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Devices with a numeric GTIN601
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. BNOS MediTECH was not found in either the U.S. or the Canadian register.

Other manufacturers in United Kingdom

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