Altius IPG Accessory Kit

FDA UDI

Class III (US FDA UDI)

by Neuros Medical, Inc.

Identity

Trade Name: Altius IPG Accessory Kit FDA UDI
Generic Name: Implantable pulse generator port plug FDA UDI
Model / Reference: FG-610-000 FDA UDI

Identifiers

Primary DI / UDI-DI: 00810118490101 FDA UDI
PMA Number: P230020 FDA UDI
FDA Product Code: SAZ FDA UDI
GMDN Term: Implantable pulse generator port plug 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Implantable pulse generator port plug

Altius IPG Accessory Kit by Neuros Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable pulse generator port plug.

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VV-PLUG — Oscor Inc. · Class III
SJM™ — ST. JUDE MEDICAL, INC. · Class III
IS4/DF4 PLUG — Oscor Inc. · Class II
Eon™ — ST. JUDE MEDICAL, INC. · Class III
Eon™ — ST. JUDE MEDICAL, INC. · Class III

Cleared under the same submission

P230020 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: Neuros Medical, Inc.

Sources (1)

FDA UDI 9596708e-4676-4c79-931b-ab6eecc4903a 33 fields · synced Jun 8, 2026