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Reverso Clamp Flow Reversing Interconnector for Hemodialysis Blood Tubing Set
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Reverso Clamp Flow Reversing Interconnector for Hemodialysis Blood Tubing Set FDA UDI
- Generic Name
- Haemodialysis blood tubing set, single-use FDA UDI
- Model / Reference
- M8-9001E FDA UDI
Identifiers
- Primary DI / UDI-DI
- M535M89001E0 FDA UDI
- FDA Product Code
- KOC FDA UDI
- GMDN Term
- Haemodialysis blood tubing set, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5820 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
Reverso Clamp Flow Reversing Interconnector for Hemodialysis Blood Tubing Set by Medisystems Corp. — Class II — FDA UDI — listed in FDA GUDID
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
- Medisystems Corp.
Sources (1)
- FDA UDI 384ef6e3-80ca-41fc-9748-376ccfbdd98d 35 fields · synced Jun 8, 2026