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Precision ™

FDA UDI

Class III (US FDA UDI)

by Boston Scientific Neuromodulation

Identity

Trade Name
Precision ™ FDA UDI
Precision ® FDA UDI
Generic Name
Implantable spinal cord electrical stimulation system programmer FDA UDI
Analgesic spinal cord electrical stimulation system FDA UDI
Device Name
Clinician Programmer Refurbished FDA UDI
Model / Reference
SC-7150R FDA UDI
Description
Clinician Programmer Refurbished FDA UDI

Identifiers

Catalog Number
SC-7150R FDA UDI
Primary DI / UDI-DI
08714729837343 FDA UDI
M365SC7150R0 FDA UDI
PMA Number
P030017 FDA UDI
FDA Product Code
LGW FDA UDI
QRB FDA UDI
GMDN Term
Implantable spinal cord electrical stimulation system programmer FDA UDI
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 UDIFDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Implantable spinal cord electrical stimulation system programmer

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

Similar devices

Also classified as Implantable spinal cord electrical stimulation system programmer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 572b1065-0f61-41a5-bb8d-7d40302fd3c2 35 fields · synced Jun 1, 2026
  • FDA UDI b7a841e5-7d03-4814-b50c-74ebf3d7171d 34 fields · synced May 22, 2026