Identity
- Trade Name
- Ritus FDA UDI
- Generic Name
- Peritoneal dialysis catheter, acute/chronic FDA UDI
- Device Name
- Peri-Patch Peritoneal Dialysis Catheter Repair Kit FDA UDI
- Model / Reference
- 8888285001 FDA UDI
- Description
- Peri-Patch Peritoneal Dialysis Catheter Repair Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10884521811546 FDA UDI
- FDA Product Code
- KGZ FDA UDI
- GMDN Term
- Peritoneal dialysis catheter, acute/chronic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
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
Ritus by Mozarc Medical US LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Peritoneal dialysis catheter, acute/chronic.
- I-SERIES PD Catheter — MEDICAL COMPONENTS INC · Class II
- I-SERIES PD CATHETER — MEDICAL COMPONENTS INC · Class II
- I-SERIES PD CATHETER — MEDICAL COMPONENTS INC · Class II
- I-SERIES PD Catheter — MEDICAL COMPONENTS INC · Class II
- V-SERIES PD Catheter — MEDICAL COMPONENTS INC · Class II
- I-SERIES PD Catheter — MEDICAL COMPONENTS INC · Class II
- V-SERIES PD Catheter — MEDICAL COMPONENTS INC · Class II
- Peritoneal Dialysis Catheter — Medionics International , Ltd. · 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mozarc Medical US LLC
Sources (1)
- FDA UDI 100fd473-6107-400b-b77f-2c67b58f01e5 34 fields · synced Jun 8, 2026