VV-Plug

FDA UDI

Class II (US FDA UDI)

by Oscor Inc.

Identity

Trade Name: VV-Plug FDA UDI
Generic Name: Implantable pulse generator port plug FDA UDI
Model / Reference: 667145-751 FDA UDI

Identifiers

Catalog Number: VV-PLUG FDA UDI
Primary DI / UDI-DI: 00885672008307 FDA UDI
510(k) Number: K031164 FDA UDI
FDA Product Code: DTD FDA UDI
GMDN Term: Implantable pulse generator port plug FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.3620 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

Dimensions & Sizes

Size: Outer Diameter — 3.2 Millimeter FDA UDI

Category: Implantable pulse generator port plug

VV-Plug by Oscor Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Implantable pulse generator port plug.

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Eon™ — ST. JUDE MEDICAL, INC. · Class III
Eon™ — ST. JUDE MEDICAL, INC. · Class III
SJM™ — ST. JUDE MEDICAL, INC. · Class III
BS DF-1 — BIOTRONIK SE & Co. KG · Class III

Cleared under the same submission

K031164 also covers:

VV-PLUG — Oscor Inc.
VV-Plug — Oscor Inc.

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 II	Pending data

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Manufacturer

Manufacturer: Oscor Inc.

Sources (1)

FDA UDI 8d4eb8b1-3914-4dba-a1b7-748e1783e670 37 fields · synced Jun 8, 2026