Identity
- Trade Name
- Red Rubber Urethral Catheters FDA UDI
- Generic Name
- Single-administration urethral drainage catheter FDA UDI
- Model / Reference
- 5066 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00616784506623 FDA UDI
- 510(k) Number
- K092250 FDA UDI
- FDA Product Code
- EYB FDA UDI
- GMDN Term
- Single-administration urethral drainage catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5130 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
Yes
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Category: Single-administration urethral drainage catheter
Red Rubber Urethral Catheters by Dynarex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Single-administration urethral drainage catheter.
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- Self-Cath — Coloplast A/S · Class II
- CURE CATHETER — CONVATEC, PURCHASING DEPARTMENT · Class II
- Apogee Plus — Hollister Incorporated · Class II
- Magic3™ Intermittent Catheter — C. R. Bard, Inc. · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- CURE ULTRA MALE CATHETER — CONVATEC, PURCHASING DEPARTMENT · Class II
Cleared under the same submission
K092250 also covers:
- Red Rubber Urethral Catheters — Dynarex Corp.
- Red Rubber Urethral Catheters — Dynarex Corp.
- Red Rubber Urethral Catheters — Dynarex Corp.
- Red Rubber Urethral Catheters — Dynarex Corp.
- Red Rubber Urethral Catheters — Dynarex Corp.
- Red Rubber Urethral Catheters — Dynarex Corp.
- Red Rubber Urethral Catheters — Dynarex Corp.
- Red Rubber Urethral Catheters — Dynarex Corp.
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
- Dynarex Corp.
Sources (1)
- FDA UDI e790a3f7-fa47-4ca5-b1be-de2224b5d664 33 fields · synced May 31, 2026