Identity
- Trade Name
- HEMO-FLOW® XF FDA UDI
- Generic Name
- Centrally-inserted central venous catheter FDA UDI
- Device Name
- 15.5F X 36CM PRE-CURVED HEMO-FLOW® XF CATHETER FULL SET (CUFF 31CM FROM TIP) FDA UDI
- Model / Reference
- MC641524 FDA UDI
- Description
- 15.5F X 36CM PRE-CURVED HEMO-FLOW® XF CATHETER FULL SET (CUFF 31CM FROM TIP) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884908084030 FDA UDI
- FDA Product Code
- FOZ FDA UDI
- GMDN Term
- Centrally-inserted central venous catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5200 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
No
FDA UDI
Hemo-Flow® Xf by Medical Components 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
- Medical Components Inc
Sources (1)
- FDA UDI a6da0d95-793b-4dee-b5fc-b89981f5e5cd 35 fields · synced Jun 8, 2026