Identity
- Trade Name
- Coiled PD Catheter FDA UDI
- Generic Name
- Peritoneal dialysis catheter, acute/chronic FDA UDI
- Device Name
- 15F X 57.5CM COILED PERITONEAL DIALYSIS CATHETER SET W/2 CUFFS FDA UDI
- Model / Reference
- MPD-257 FDA UDI
- Description
- 15F X 57.5CM COILED PERITONEAL DIALYSIS CATHETER SET W/2 CUFFS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884908030877 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
- 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
Coiled PD Catheter by Medical Components Inc — Class II — 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medical Components Inc
Sources (1)
- FDA UDI 1034d205-a879-4f6d-9812-9a315d9e9e52 35 fields · synced May 30, 2026