Identity
- Trade Name
- COMPACTCATH Extension Tube FDA UDI
- Generic Name
- Urinary catheter/drainage bag connection facilitator FDA UDI
- Device Name
- The CompactCath extension tube is connect with CompactCath Lubricated Intermittent Urinary Catheter when needed. FDA UDI
- Model / Reference
- 1903-1832 FDA UDI
- Description
- The CompactCath extension tube is connect with CompactCath Lubricated Intermittent Urinary Catheter when needed. FDA UDI
Identifiers
- Catalog Number
- 1903-1832 FDA UDI
- Primary DI / UDI-DI
- 10852141007847 FDA UDI
- FDA Product Code
- KNX FDA UDI
- GMDN Term
- Urinary catheter/drainage bag connection facilitator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5250 FDA UDI
- Commercial Distribution
- 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
Yes
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 — 16 French FDA UDILength — 16 Inch FDA UDI
Category: Urinary catheter/drainage bag connection facilitator
COMPACTCATH Extension Tube by Compactcath, 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 |
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Manufacturer
- Manufacturer
- Compactcath, Inc
Sources (1)
- FDA UDI 715c853d-6f1a-4b4c-bac6-61388c0d12f6 36 fields · synced Jun 1, 2026