Beamer
by Conmed Corporation United States EUDAMEDGUDID
Ref A-BEAM-1, BEAMSNARE-1, A-BEAM-4, S-BEAM-3, AVEO-1W, BEAMSNARE-2, BEAMSNARE-3, A-BEAM-3, AVEO-TANK-LRG, A-BEAM-5
Product code GEIEMDN K0204010101
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-20653405056437 | Date13 Apr 2026 | StatusActive |
| United States | GUDID listing GUDID | Number20653405056437 | Date24 Sep 2016 | StatusIn distribution |
Coverage
- Expiring (legacy directive)
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- BeamerBeamer AVEO
- Generic Name
- Inert gas-enhanced endoscopic electrosurgical electrode, single-useFoot-switch, electricalMedical device integration rack
- Device Name
- Non-orthopedic, Active, Instrument, Electrosurgical, Endoscopic, Beamer Argon ProbeNon-orthopedic, Active, Instrument, Electrosurgical, Endoscopic, Beamer Argon Snare ProbeNon-orthopedic, Active, Electrosurgical Generator, Argon, Endoscopic
- Model / Ref / Catalog
- A-BEAM-1, BEAMSNARE-1, A-BEAM-4, S-BEAM-3, AVEO-1W, BEAMSNARE-2, BEAMSNARE-3, A-BEAM-3, A-BEAM-5, AVEO-TANK-LRG
- Primary DI / UDI-DI
- 20653405056437, 20653405064166, 20653405056451, 10653405986461, 20845854082376, 20653405064173, 20653405064180, 20653405056468, 20653405056475, 30845854082830
- Basic UDI-DI
- B-20653405056437, B-20653405064166, B-20653405056451, B-10653405986461, 084585464930EY, B-20653405064173, B-20653405064180, B-20653405056468, B-20653405056475
- Direct Marketing DI
- 1084585408237910845854082836
- FDA Product Code
- GEI
- EMDN Code
- K0204010101, Z12021199, Z129099, Z12029099
- GMDN Term
- Inert gas-enhanced endoscopic electrosurgical electrode, single-useFoot-switch, electricalMedical device integration rack
- Device Class
- Class IIb EUDAMEDClass I EUDAMEDClass II GUDID
- Regulation Number
- 878.4400
- Market of Registration
- Belgium
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Ethylene Oxide
- Size
- Length — 160 CentimeterWidth — 2.5 MillimeterLength — 230 Centimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIb Class I | Class II |
Manufacturer details
- EUDAMED SRN
- US-MF-000012663
- Authorised representative
- MDSS GmbH DE-AR-000005430
Other devices from Conmed Corporation
Properties & raw data
Show properties, registry sources and raw records
Other properties (17)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
Sources (20)
- EUDAMED 16c00fd7-7eb3-4855-ab32-15ad8f098630
- EUDAMED 20653405064166|B-20653405064166
- EUDAMED 20653405056451|B-20653405056451
- EUDAMED 10653405986461|B-10653405986461
- EUDAMED 20845854082376|084585464930EY
- EUDAMED 20653405064173|B-20653405064173
- EUDAMED 20653405064180|B-20653405064180
- EUDAMED 20653405056468|B-20653405056468
- FDA UDI af1209c5-a50e-4bd1-8395-3e822dffd8ef
- FDA UDI c4264740-f89f-4e58-83d0-acd53461891d
- FDA UDI 138449da-4858-4a76-a53b-bab085a24611
- FDA UDI 81daad64-fa4c-4920-8200-587accbdc94f
- FDA UDI 7feea6de-b4af-4d8e-ae7e-3c672810c8ba
- FDA UDI 5c82fd00-260f-40b6-b295-6c6cd908c0e2
- FDA UDI 2b59c9cc-cbc6-4297-ae93-17a9ff545ca8
- FDA UDI 92c5a108-a1ce-4c61-983b-522dd1cab153
- FDA UDI 593deb22-040d-4380-b8ef-efd9f737de5b
- FDA UDI 852a29be-e811-4005-bfa5-9f2a3e9b9a89
- EUDAMED 30845854082830|084585464930EY
- EUDAMED 20653405056475|B-20653405056475