Identity
- Trade Name
- MAHURKAR FDA UDI
- Generic Name
- Double-lumen haemodialysis catheter, nonimplantable FDA UDI
- Device Name
- Acute Dual Lumen Catheter Tray,High Flow Pre-Curved with IC* Components,13.5 Fr/Ch (4.5 mm) x 24 cm FDA UDI
- Model / Reference
- 8888135246 FDA UDI
- Description
- Acute Dual Lumen Catheter Tray,High Flow Pre-Curved with IC* Components,13.5 Fr/Ch (4.5 mm) x 24 cm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10884521006584 FDA UDI
- FDA Product Code
- MPB FDA UDI
- GMDN Term
- Double-lumen haemodialysis catheter, nonimplantable 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
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Catheter Gauge — 13.5 French FDA UDILength — 24 Centimeter FDA UDI
Mahurkar by Mozarc Medical US LLC — 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 |
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Manufacturer
- Manufacturer
- Mozarc Medical US LLC
Sources (1)
- FDA UDI 246f3a95-f9d4-4388-a4e0-657a834ff590 36 fields · synced Jun 8, 2026