FDA UDI
In Commercial Distribution
🇺🇸 United States
NociRelief
DI: 08908006064212
·
Model: NociRelief
·
DYANSYS INDIA PRIVATE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- NociRelief
- Primary DI
- 08908006064212
- Version / Model
- NociRelief
- Company Name
- DYANSYS INDIA PRIVATE LIMITED
- Labeler DUNS
- 916731981
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2026-03-16
- Public Version
- 1
- Public Version Date
- 2026-03-24
- Public Version Status
- New
- Public Device Record Key
- a15efea9-718c-419c-911a-3e99f3f8f177
Device Description
NociRelief
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| NHI | Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief | Neurology | 882.5890 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 67067 | Analgesic periauricular vagus nerve percutaneous electrical stimulator | A body-worn electronic device intended for vagus nerve stimulation (VNS) applied close to auricular peripheral nerves to achieve remote pain relief mediated by central nervous system (CNS) pathways and structures [e.g., brainstem activation]; it may be used to relieve chronic pain (e.g., back pain, cervical syndrome, migraine) or acute pain (e.g., post-operative pain). It consists of an electrical pulse generator with minimally-invasive electrodes intended to be applied to the auricle by a clinical professional. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 08908006064212 | GS1 |