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Microwave Ablation Generator

EUDAMEDFDA UDIFDA 510(k)

Class IIb (EU MDR)

Ref KY-2000A510(k) K241827Ref H-1

by Canyon Medical Inc.

Identity

Trade Name
Microwave Ablation Generator EUDAMEDFDA UDI
Generic Name
Microwave hyperthermia system FDA UDI
Device Name
Microwave Ablation Generator EUDAMEDFDA UDI
Model / Reference
KY-2000A EUDAMEDFDA UDI
H-1 EUDAMED
Description
Microwave Ablation Generator FDA UDI

Identifiers

Primary DI / UDI-DI
06954414610024 EUDAMEDFDA UDI
06954414610017 EUDAMED
Basic UDI-DI
6954414600100001ED EUDAMED
6954414600100002EF EUDAMED
Direct Marketing DI
06954414610024 EUDAMED
06954414610017 EUDAMED
510(k) Number
K241827 FDA UDI
FDA Product Code
NEY FDA UDI
EMDN Code
Z120608 MICROWAVE THERAPY EQUIPMENT EUDAMED
GMDN Term
Microwave hyperthermia system FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDEUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Microwave ablation system probe, non-powered

Microwave Ablation Generator by Canyon Medical Inc. — Class IIb — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system probe, non-powered.

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Canyon Medical Inc.
EUDAMED SRN
CN-MF-000022663
FDA Applicant
Canyon Medical, Inc.
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (4)

  • EUDAMED f5bdebe8-97c9-44a3-ad61-ace3f4794ca6 85 fields · synced Aug 2, 2026
  • EUDAMED 0a64d336-6b13-4b92-b1b9-6b405efbe185 61 fields · synced May 17, 2026
  • FDA UDI f3c4da32-71bf-4e71-bfde-fb46d814534b 34 fields · synced May 29, 2026
  • FDA 510(k) K241827 1 fields · synced May 18, 2026