← Back to catalogue

Precision®, NA

FDA UDI

Class III (US FDA UDI)

by Boston Scientific Neuromodulation

Identity

Trade Name
Precision®, NA FDA UDI
Generic Name
Analgesic spinal cord electrical stimulation system FDA UDI
Device Name
Remote Control Silicone Case Royal Blue FDA UDI
Model / Reference
NM-6215-BL2 FDA UDI
Description
Remote Control Silicone Case Royal Blue FDA UDI

Identifiers

Catalog Number
NM-6215-BL2 FDA UDI
Primary DI / UDI-DI
M365NM6215BL20 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

Yes

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

Yes

FDA UDI

Category: Analgesic spinal cord electrical stimulation system

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

Similar devices

Also classified as Analgesic spinal cord electrical stimulation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 50373d35-021e-4bee-9b1a-dc5b7bb03b09 34 fields · synced May 31, 2026