Identity
- Trade Name
- Optiflux® Ultra FDA UDI
- Generic Name
- Hollow-fibre haemodialysis dialyser, single-use FDA UDI
- Device Name
- F190 Optiflux Ultra Dialyzer / High Flux / Polysulfone / 1.9 m2 / Ebeam / Single Use / 105 mL FDA UDI
- Model / Reference
- 0500419E FDA UDI
- Description
- F190 Optiflux Ultra Dialyzer / High Flux / Polysulfone / 1.9 m2 / Ebeam / Single Use / 105 mL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840861100200 FDA UDI
- FDA Product Code
- KDI FDA UDI
- GMDN Term
- Hollow-fibre haemodialysis dialyser, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5860 FDA UDI
- Commercial Distribution
- Not 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Area/Surface Area — 1.9 Square meter FDA UDI
Optiflux® Ultra by Fresenius Medical Care Holdings, Inc. — 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
- Fresenius Medical Care Holdings, Inc.
Sources (1)
- FDA UDI 0e2570e0-e4b7-429a-a717-4ba4e70d8c3b 37 fields · synced Jun 1, 2026