N'vision™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name: N'VISION™ FDA UDI
Generic Name: Multiple active implantable device programmer FDA UDI
Device Name: PRGMR 8840 N'VISION PHYSICN W LOANER INS FDA UDI
Model / Reference: 8840 FDA UDI
Description: PRGMR 8840 N'VISION PHYSICN W LOANER INS FDA UDI

Identifiers

Primary DI / UDI-DI: 00613994997845 FDA UDI
PMA Number: P080025 FDA UDI
P840001 FDA UDI
P860004 FDA UDI
P960009 FDA UDI
P970004 FDA UDI
FDA Product Code: MHY FDA UDI
LGW FDA UDI
LNQ FDA UDI
MRU FDA UDI
LKK FDA UDI
MFR FDA UDI
EZW FDA UDI
OLM FDA UDI
NHL FDA UDI
QON FDA UDI
PJS FDA UDI
QRB FDA UDI
GMDN Term: Multiple active implantable device programmer FDA UDI

Classification

Device Class: Class III 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 III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

P080025 also covers:

P840001 also covers:

P860004 also covers:

P960009 also covers:

P970004 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: Medtronic, Inc.

Sources (1)

FDA UDI 4c127bad-576b-4ba3-8976-2f26be215335 36 fields · synced Jun 6, 2026