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Bionic Navigator™ 3D

FDA UDI

Class III (US FDA UDI)

by Boston Scientific Neuromodulation

Identity

Trade Name
Bionic Navigator™ 3D FDA UDI
Generic Name
Implantable electrical stimulation device management software FDA UDI
Device Name
2.10 Installer FDA UDI
Model / Reference
SC-7101-210-W10 FDA UDI
Description
2.10 Installer FDA UDI

Identifiers

Primary DI / UDI-DI
08714729991373 FDA UDI
PMA Number
P030017 FDA UDI
FDA Product Code
LGW FDA UDI
QRB FDA UDI
GMDN Term
Implantable electrical stimulation device management software FDA UDI

Classification

Device Class
Class III 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Implantable electrical stimulation device management software

Bionic Navigator™ 3D by Boston Scientific Neuromodulation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable electrical stimulation device management software.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cacd8599-5528-495f-a139-6c9e808c6595 34 fields · synced May 30, 2026