Identity
- Trade Name
- Porges Coloplast FDA UDI
- Generic Name
- Polymeric ureteral stent FDA UDI
- Device Name
- Double loop ureteral stent in silicone open/closed CH FR 08 length 26 cm with connectable pusher and fixed core guidewire FDA UDI
- Model / Reference
- AJ4884 FDA UDI
- Description
- Double loop ureteral stent in silicone open/closed CH FR 08 length 26 cm with connectable pusher and fixed core guidewire FDA UDI
Identifiers
- Catalog Number
- AJ4884 FDA UDI
- Primary DI / UDI-DI
- 03600040201237 FDA UDI
- FDA Product Code
- FAD FDA UDI
- GMDN Term
- Polymeric ureteral stent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4620 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
Dimensions & Sizes
- Size
- Catheter Gauge — 8 French FDA UDILength — 26 Centimeter FDA UDI
Porges Coloplast by Coloplast A/S — 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
- Coloplast A/S
Sources (1)
- FDA UDI fba058a5-260f-46c3-862c-4c29c6fe4f6f 38 fields · synced Jun 6, 2026