N'vision®

FDA UDI

Class Unclassified (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name: N'VISION® FDA UDI
Generic Name: Multiple active implantable device programmer FDA UDI
Device Name: SW 8870MMC01 NVISION INTSTM ENTERRA2 US FDA UDI
Model / Reference: 8870MMC01 FDA UDI
Description: SW 8870MMC01 NVISION INTSTM ENTERRA2 US FDA UDI

Identifiers

Primary DI / UDI-DI: 00643169427037 FDA UDI
FDA Product Code: LNQ FDA UDI
EZW FDA UDI
QON FDA UDI
GMDN Term: Multiple active implantable device programmer FDA UDI

Classification

Device Class: Unclassified FDA UDI
Regulation Number: 876.5270 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Multiple active implantable device programmer

N'vision® by Medtronic, Inc. — Class Unclassified — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 Unclassified	Pending data

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Manufacturer

Manufacturer: Medtronic, Inc.

Sources (1)

FDA UDI e4bd0293-0fec-4973-b006-39667369400d 35 fields · synced Jun 1, 2026