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Curaway

FDA UDI

Class II (US FDA UDI)

by Zhejiang CuraWay Medical Technology Co., Ltd.

Identity

Trade Name
Curaway FDA UDI
Generic Name
Peripheral vascular electrocautery catheter, single-use FDA UDI
Device Name
Endovenous Radiofrequency Catheter FDA UDI
Model / Reference
CFB 2.3-7-100 FDA UDI
Description
Endovenous Radiofrequency Catheter FDA UDI

Identifiers

Primary DI / UDI-DI
06936666559337 FDA UDI
510(k) Number
K232505 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Peripheral vascular electrocautery catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Peripheral vascular electrocautery catheter, single-use

Curaway by Zhejiang CuraWay Medical Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular electrocautery catheter, single-use.

Cleared under the same submission

K232505 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zhejiang CuraWay Medical Technology Co., Ltd.

Sources (1)

  • FDA UDI 7b9b06e0-1820-45e3-9deb-7a7d0250b6ad 34 fields · synced May 30, 2026