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Silicone Hemo Cath-No Cuff/Acutesilicone Hemo Cath-No Cuff/Acute
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- SILICONE HEMO CATH-NO CUFF/ACUTESILICONE HEMO CATH-NO CUFF/ACUTE FDA UDI
- Generic Name
- Double-lumen haemodialysis catheter, implantable FDA UDI
- Device Name
- 11.5F X 20CM HEMO-CATH® SILICONE DOUBLE LUMENSILICONE DO CATHETER W/STYLETCATHETER W/STYL FDA UDI
- Model / Reference
- DSL20C FDA UDI
- Description
- 11.5F X 20CM HEMO-CATH® SILICONE DOUBLE LUMENSILICONE DO CATHETER W/STYLETCATHETER W/STYL FDA UDI
Identifiers
- Catalog Number
- DSL20C FDA UDI
- Primary DI / UDI-DI
- 00884908141771 FDA UDI
- FDA Product Code
- LFJ FDA UDI
- GMDN Term
- Double-lumen haemodialysis catheter, implantable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5540 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
Silicone Hemo Cath-No Cuff/Acutesilicone Hemo Cath-No Cuff/Acute by Medical Components Inc — 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
- Medical Components Inc
Sources (1)
- FDA UDI 694cf9f1-53e9-4e99-8f1d-dc75e474dc85 36 fields · synced May 30, 2026