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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
PROGRAMMER 8840 CLINICIAN REFURB US FDA UDI
Model / Reference
8840-RFB FDA UDI
Description
PROGRAMMER 8840 CLINICIAN REFURB US FDA UDI

Identifiers

Primary DI / UDI-DI
00763000875862 FDA UDI
PMA Number
H020007 FDA UDI
H050003 FDA UDI
P080025 FDA UDI
P840001 FDA UDI
P860004 FDA UDI
P960009 FDA UDI
P970004 FDA UDI
FDA Product Code
LGW FDA UDI
NHL FDA UDI
OLM FDA UDI
MHY FDA UDI
PJS FDA UDI
QON FDA UDI
EZW FDA UDI
LKK FDA UDI
LNQ FDA UDI
MRU 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

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

Similar devices

Also classified as Multiple active implantable device programmer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 6e515998-2553-47cf-bf0f-2914c24e7d7f 36 fields · synced Jun 1, 2026