Identity
- Trade Name
- Dash 6 FDA UDI
- Generic Name
- Neuraxial syringe FDA UDI
- Device Name
- Dash 6, Lock Syringes, NRFit® Syringes, Single Use 20ml (BNS) FDA UDI
- Model / Reference
- 15010200 FDA UDI
- Description
- Dash 6, Lock Syringes, NRFit® Syringes, Single Use 20ml (BNS) FDA UDI
Identifiers
- Catalog Number
- 15010200 FDA UDI
- Primary DI / UDI-DI
- 05060498307093 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- Neuraxial syringe FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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 UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Dash 6 by Intervene Group Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Intervene Group Limited
Sources (1)
- FDA UDI db54ffe0-c1b9-4310-a41f-2b9c2a72bc69 35 fields · synced May 30, 2026