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FDA product code PZR

Percutaneous Nerve Stimulator For Opioid Withdrawal

NeurologyClass 221 CFR 882.5896
Verified
US regulatory classifications
US Product Code (FDA)
PZR
View Product Code Classification
US Risk Class (FDA)
Class 2
US Regulation (CFR)
21 CFR 882.5896
View CFR Regulation
Medical specialty
Neurology
Device characteristics
GMP exempt
No
Implantable
No
Life-sustaining
No
Third party review
Not Eligible
Definition

Stimulate nerve branches to aid in the reduction of symptoms associated with substance use disorders.

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01Nerve stimulator02Opioid withdrawal03Addiction treatment04Percutaneous stim05Neuro stimulator06Detox device07Pain relief08Auricular stim09Drug withdrawal10Rehabilitation device
About this record

Percutaneous Nerve Stimulator For Opioid Withdrawal is a medical device type in the Neurology specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.