Identity
- Trade Name
- N/AN/A FDA UDI
- Generic Name
- Centrally-inserted central venous catheter FDA UDI
- Device Name
- 7F X 20CM TRIPLE LUMEN7F X 20CM INFUSION CATHETER KITINFUSION CA FDA UDI
- Model / Reference
- MC3L-8K FDA UDI
- Description
- 7F X 20CM TRIPLE LUMEN7F X 20CM INFUSION CATHETER KITINFUSION CA FDA UDI
Identifiers
- Catalog Number
- MC3L-8K FDA UDI
- Primary DI / UDI-DI
- 00884908029048 FDA UDI
- FDA Product Code
- JCY FDA UDI
- GMDN Term
- Centrally-inserted central venous catheter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 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
Yes
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
N/An/A by Medical Components Inc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Medical Components Inc
Sources (1)
- FDA UDI 6e6bb192-e0b8-4d72-9faf-2b755b243522 36 fields · synced May 30, 2026