Identity
- Trade Name
- CAPIOX® HEMOCONCENTRATOR FDA UDI
- Generic Name
- Haemoconcentrator FDA UDI
- Model / Reference
- CX*HC11L FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04987350738417 FDA UDI
- FDA Product Code
- KDI FDA UDI
- GMDN Term
- Haemoconcentrator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5860 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
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 — 1.1 Square meter FDA UDI
Category: Haemoconcentrator
Capiox® Hemoconcentrator by Terumo Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Haemoconcentrator.
- DHF — SORIN GROUP ITALIA SRL · Class II
- DHF — SORIN GROUP ITALIA SRL · Class II
- SH — SORIN GROUP ITALIA SRL · Class II
- CAPIOX® HEMOCONCENTRATOR — Terumo Corp. · Class II
- CAPIOX® HEMOCONCENTRATOR — Terumo Corp. · Class II
- CAPIOX® HEMOCONCENTRATOR — Terumo Corp. · 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
- Terumo Corp.
Sources (1)
- FDA UDI 34808744-364a-4454-a367-8df3a9cd1ebe 35 fields · synced May 31, 2026