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Venclose Maven Catheter

FDA UDI

Class II (US FDA UDI)

by Venclose Inc

Identity

Trade Name
Venclose Maven Catheter FDA UDI
Generic Name
Peripheral vascular electrocautery catheter, single-use FDA UDI
Device Name
Venclose Perforator Catheter FDA UDI
Model / Reference
VC056F FDA UDI
Description
Venclose Perforator Catheter FDA UDI

Identifiers

Primary DI / UDI-DI
00858254006398 FDA UDI
510(k) Number
K211806 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Peripheral vascular electrocautery catheter, single-use

Venclose Maven Catheter by Venclose Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Venclose Inc

Sources (1)

  • FDA UDI 6631a424-009a-4f6b-94c9-7d19fa8d994d 34 fields · synced Jun 8, 2026