Identity
- Trade Name
- V-SERIES PD Catheter FDA UDI
- Generic Name
- Peritoneal dialysis catheter, acute/chronic FDA UDI
- Device Name
- 15F X 63CM V-SERIES COILED DIALYSIS CATHETER LEFT W/ 2 CUFFS (CATHETER ONLY) FDA UDI
- Model / Reference
- MC20VC63LC FDA UDI
- Description
- 15F X 63CM V-SERIES COILED DIALYSIS CATHETER LEFT W/ 2 CUFFS (CATHETER ONLY) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884908092226 FDA UDI
- FDA Product Code
- FJS FDA UDI
- GMDN Term
- Peritoneal dialysis catheter, acute/chronic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5630 FDA UDI
- Commercial Distribution
- 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
Category: Peritoneal dialysis catheter, acute/chronic
V-SERIES PD Catheter by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Peritoneal dialysis catheter, acute/chronic.
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- Argyle — Mozarc Medical US LLC · Class II
- Argyle — Mozarc Medical US LLC · Class II
- Argyle — Mozarc Medical US LLC · Class II
- Argyle — Mozarc Medical US LLC · Class II
- Argyle — Mozarc Medical US LLC · Class II
- Argyle — Mozarc Medical US LLC · 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
- Medical Components Inc
Sources (1)
- FDA UDI dfb69e1d-8044-4b48-b46d-6b2416ad5921 34 fields · synced Jun 8, 2026