Identity
- Trade Name
- Ethox FDA UDI
- Generic Name
- Intravenous pressure infusor, manual, reusable FDA UDI
- Device Name
- 3000 ml Disposable Pressure Infuser FDA UDI
- Model / Reference
- VC430 FDA UDI
- Description
- 3000 ml Disposable Pressure Infuser FDA UDI
Identifiers
- Catalog Number
- VC430 FDA UDI
- Primary DI / UDI-DI
- 10889483110782 FDA UDI
- FDA Product Code
- KZD FDA UDI
- GMDN Term
- Intravenous pressure infusor, manual, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5420 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
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 3000 Milliliter FDA UDI
Ethox by Ethox Medical, Llc — Class I — 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ethox Medical, Llc
Sources (1)
- FDA UDI 95373dc2-049b-47e9-b138-f1c956f1c0da 37 fields · synced May 30, 2026