FDA.reportPublic FDA data

Curaway

Primary DI
06936666559528
Brand
Curaway
Company
Zhejiang CuraWay Medical Technology Co., Ltd.
Model
CFD 1.6-1-60
Device description
Endovenous Radiofrequency Catheter
Published
2025-09-05
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
GEIElectrosurgical, Cutting & Coagulation & Accessories

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEIElectrosurgical, Cutting & Coagulation & AccessoriesGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K232505000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K232505000Endovenous Radiofrequency Generator, Endovenous Radiofrequency CatheterZhejiang Curaway Medical Technology Co., Ltd.2024-05-30GEI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
16936666559525PackageGS110In Commercial Distribution
06936666559528PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1693666655952516936666559525
06936666559528069366665595286936666559528

GMDN Terms#

Term, Definition table
TermDefinition
Peripheral vascular electrocautery catheter, single-useA flexible catheter with a distal heating element/electrode intended to be connected to an electrical generator and introduced into the peripheral vasculature to ablate venous tissues, through direct application of heat, as a treatment for venous reflux disease (varicose veins); it is not intended to introduce electrical current into the body. It is a luminal device with a proximal handle with controls (e.g., on/off switch) that is introduced via an introducer assembly (which may be included), and is typically maneuvered under external image guidance [e.g., ultrasound (US)]. This is a single-use device.

Regulatory Flags#

DUNS number
412923111
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
06937278635983CurawayBN-OCR-1/14082026-05-31
06937278635990CurawayBN-OCR-1/14092026-05-31
06937278636003CurawayBN-OCR-1/14102026-05-31
06937278636010CurawayBN-OCR-1/14132026-05-31
06937278636027CurawayBN-OCR-1/14152026-05-31
06937278636034CurawayBN-OCR-1/14162026-05-31
06937278636041CurawayBN-OCR-1/14182026-05-31
06937278636058CurawayBN-OCR-1/14202026-05-31
06937278636065CurawayBN-OCR-1/14252026-05-31
06937278636072CurawayBN-OCR-1/16082026-05-31
06937278636089CurawayBN-OCR-1/16092026-05-31
06937278636096CurawayBN-OCR-1/16102026-05-31
06937278636102CurawayBN-OCR-1/16132026-05-31
06937278636119CurawayBN-OCR-1/16152026-05-31
06937278636126CurawayBN-OCR-1/16162026-05-31
06937278636133CurawayBN-OCR-1/16182026-05-31
06937278636140CurawayBN-OCR-1/16202026-05-31
06937278636157CurawayBN-OCR-1/16252026-05-31
06937278636164CurawayBN-OCR-1/18082026-05-31
06937278636171CurawayBN-OCR-1/18092026-05-31

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08809306764140VIVA RF ElectrodeSTARMED CO.,LTDGEI2026-06-04
08809306764157VIVA RF ElectrodeSTARMED CO.,LTDGEI2026-06-04
08809306764164VIVA RF ElectrodeSTARMED CO.,LTDGEI2026-06-04
08809306764171VIVA RF ElectrodeSTARMED CO.,LTDGEI2026-06-04
08809306764188VIVA RF ElectrodeSTARMED CO.,LTDGEI2026-06-04
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