← Back to catalogue

ClosureRFS

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
ClosureRFS FDA UDI
Generic Name
Peripheral vascular electrocautery catheter, single-use FDA UDI
Device Name
Endovenous Radiofrequency Stylet,6 Fr/Ch (2.0 mm) x 12 cm FDA UDI
Model / Reference
RFS2-6-12 FDA UDI
Description
Endovenous Radiofrequency Stylet,6 Fr/Ch (2.0 mm) x 12 cm FDA UDI

Identifiers

Primary DI / UDI-DI
10884521058095 FDA UDI
510(k) Number
K052003 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

Dimensions & Sizes

Size
Catheter Gauge — 6 French FDA UDI
Length — 12 Centimeter FDA UDI

Category: Peripheral vascular electrocautery catheter, single-use

ClosureRFS by Covidien LP — 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

K052003 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 072dcd15-f2ff-430a-8c33-0f544761eca5 37 fields · synced Jun 1, 2026