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Bionic Navigator™ 3D

FDA UDIEUDAMED

Class III (US FDA UDI)

by Boston Scientific Neuromodulation

Identity

Trade Name
Bionic Navigator™ 3D FDA UDI
Generic Name
Analgesic spinal cord electrical stimulation system FDA UDI
Device Name
2.10 Installer FDA UDI
Model / Reference
SC-7101-210 FDA UDI
Description
2.10 Installer FDA UDI

Identifiers

Primary DI / UDI-DI
08714729970606 FDA UDI
PMA Number
P030017 FDA UDI
FDA Product Code
LGW FDA UDI
GMDN Term
Analgesic spinal cord electrical stimulation system 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: Analgesic spinal cord electrical stimulation system

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

Similar devices

Also classified as Analgesic spinal cord electrical stimulation system.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 6c6c2de7-8f6d-4f1d-9ce3-e56f1dc27b17 34 fields · synced Jun 1, 2026
  • EUDAMED 1 fields · synced May 29, 2026