Identity
- Trade Name
- Scorpion FDA UDI
- Generic Name
- Nerve-locating system probe, single-use FDA UDI
- Device Name
- Single-Use Scorpion Stimulation Foreceps 1 pc FDA UDI
- Model / Reference
- I-D-WSF512 FDA UDI
- Description
- Single-Use Scorpion Stimulation Foreceps 1 pc FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08720791370794 FDA UDI
- FDA Product Code
- GXZ FDA UDI
- GMDN Term
- Nerve-locating system probe, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Nerve-locating system probe, single-use
Scorpion by Technomed Engineering B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Nerve-locating system probe, single-use.
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- Scorpion — NEUROVISION MEDICAL PRODUCTS, INC. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Technomed Engineering B.V.
Sources (1)
- FDA UDI 3af2e5a9-d62a-4f7a-ac62-59a62e42eb08 34 fields · synced May 31, 2026