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Oxo 300

EUDAMED

Class IIb (EU MDR)

Ref 122256 V1 / BMK3-100-300 + M74200002Ref 122250 V1Ref 122220 V1 / ULC1-79-300 + M74200002Ref 122230 V2 / MMC2-88-300 + M742000005Ref 122230 V1 / BMK2-88-300 + M74200005Ref 122256 V2 / MMC2-88-300 + M74200002

by EMS GmbH Emergency Medical Systems

Identity

Trade Name
OXO 300 EUDAMED
Device Name
1222250 V1 EUDAMED
Model / Reference
122256 V1 / BMK3-100-300 + M74200002 EUDAMED
122250 V1 EUDAMED
122220 V1 / ULC1-79-300 + M74200002 EUDAMED
122230 V2 / MMC2-88-300 + M742000005 EUDAMED
122230 V1 / BMK2-88-300 + M74200005 EUDAMED
122256 V2 / MMC2-88-300 + M74200002 EUDAMED

Identifiers

Primary DI / UDI-DI
04262455360023 EUDAMED
04262455360016 EUDAMED
04262455360078 EUDAMED
04262455360061 EUDAMED
04262455360054 EUDAMED
04262455360030 EUDAMED
Basic UDI-DI
426245536OXOBasic1CM EUDAMED
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Medical Purpose
This cylinder valve with integrated regulator and integrated residual pressure valve device is design for oxygen therapy. This Ceodeux S.A. Meditec product will regulate the high pressure of the medical oxygen gas cylinder and deliver it to the patient. This PRODUCT is not intended for any other installation or purpose. If the product user has any question regarding this PRODUCT’s proper application or purpose, the product user should call *352 327832-1 or Fax * 352-32.78.32.317. Any non-approved use or application and/or any non-approved modification of the PRODUCT or its use or application may result in a serious accident or personal injury for which CEODEUX S.A will not be responsible. Ceodeux S.A cannot be held responsible for an inappropriate use of the product. The supplier of the final equipment is responsible for the homologation of the system. CEODEUX S.A. cannot be held responsible of the latter’s negligence. Recommendations of CODEUX S.A. do not substitute for the final responsibility of a customer. EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Oxo 300 by EMS GmbH Emergency Medical Systems — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
EMS GmbH Emergency Medical Systems
EUDAMED SRN
DE-PR-000040122

Sources (6)

  • EUDAMED a954a971-4db5-4314-a8d7-a2cc2340cd6c 61 fields · synced Jul 31, 2026
  • EUDAMED 267559f8-eb49-489d-88b6-b38d751a56c0 61 fields · synced May 17, 2026
  • EUDAMED 0d9c922c-d8aa-4d6e-b209-4d12a01c8c27 61 fields · synced May 18, 2026
  • EUDAMED dad447b7-3152-4b43-ac08-2e47877e7b49 61 fields · synced May 18, 2026
  • EUDAMED 08b75e6e-eee0-461d-97b8-97e6b205097f 61 fields · synced May 18, 2026
  • EUDAMED 686c91bb-a916-47ee-bbb2-262b01cedbd3 61 fields · synced May 19, 2026