Identity
- Trade Name
- Porges Coloplast FDA UDI
- Generic Name
- Ureteral introduction sheath FDA UDI
- Device Name
- Retrace Ureteral Accesss Sheath 35cm FDA UDI
- Model / Reference
- ACXL12 FDA UDI
- Description
- Retrace Ureteral Accesss Sheath 35cm FDA UDI
Identifiers
- Catalog Number
- ACXL12 FDA UDI
- Primary DI / UDI-DI
- 03600040274583 FDA UDI
- FDA Product Code
- FED FDA UDI
- GMDN Term
- Ureteral introduction sheath FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
No
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 — 14 French FDA UDICatheter Gauge — 12 French 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 89f7a50c-aa77-46c6-8345-45a1bbb04d7b 38 fields · synced Jun 1, 2026