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Precision™ Montage™ MRI

FDA UDI

Class III (US FDA UDI)

by Boston Scientific Neuromodulation

Identity

Trade Name
Precision™ Montage™ MRI FDA UDI
Generic Name
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable FDA UDI
Device Name
Implantable Pulse Generator Kit FDA UDI
Model / Reference
SC-1200 FDA UDI
Description
Implantable Pulse Generator Kit FDA UDI

Identifiers

Primary DI / UDI-DI
08714729905943 FDA UDI
PMA Number
P030017 FDA UDI
FDA Product Code
LGW FDA UDI
QRB FDA UDI
GMDN Term
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable

Precision™ Montage™ MRI by Boston Scientific Neuromodulation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable.

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 c0c2d3a0-ab32-4dc5-9d23-a660cfcf42db 34 fields · synced Jun 8, 2026