Vega

FDA UDI

Class III (US FDA UDI)

by Microport Crm Srl

Identity

Trade Name: Vega FDA UDI
Generic Name: Pacing/defibrillation lead stylet FDA UDI
Device Name: VEGA Stylet Kit 52cm FDA UDI
Model / Reference: RLK41U FDA UDI
Description: VEGA Stylet Kit 52cm FDA UDI

Identifiers

Catalog Number: RLK41U FDA UDI
Primary DI / UDI-DI: 08031527019826 FDA UDI
PMA Number: P130010 FDA UDI
FDA Product Code: NVN FDA UDI
GMDN Term: Pacing/defibrillation lead stylet FDA UDI

Classification

Device Class: Class III FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pacing/defibrillation lead stylet

Vega by Microport Crm Srl — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

P130010 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: Microport Crm Srl

Sources (1)

FDA UDI a1b87487-22a7-480f-a763-c08bfa16d028 36 fields · synced Jun 8, 2026