Identity
- Trade Name
- Hollister EUDAMEDVaPro FDA UDI
- Generic Name
- Single-administration urethral drainage catheter FDA UDI
- Device Name
- No Touch Urethral Intermittent Catheter, Nelaton EUDAMEDNo Touch Urethral Intermittent Catheter, Hydrophilic, Straight Tip, Protective Tip and Sleeve FDA UDI
- Model / Reference
- 72142 EUDAMEDFDA UDI
- Description
- No Touch Urethral Intermittent Catheter, Hydrophilic, Straight Tip, Protective Tip and Sleeve FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00610075081240 EUDAMEDFDA UDI
- Basic UDI-DI
- 610075D03P081S0258C4 EUDAMED
- Unit of Use DI
- 00610075065431 EUDAMED
- 510(k) Number
- K141642 FDA UDI
- FDA Product Code
- GBM FDA UDI
- EMDN Code
- U01010501 NELATON CATHETERS, SELF-LUBRICATING EUDAMED
- GMDN Term
- Single-administration urethral drainage catheter FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.5130 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
Yes
Dimensions & Sizes
- Size
- Length — 8 Inch FDA UDICatheter Gauge — 14 French FDA UDI
Category: Intermittent urethral drainage catheter, non-antimicrobial, single-use
Hollister by Hollister Incorporated — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intermittent urethral drainage catheter, non-antimicrobial, single-use.
- Sterile Urinary Catheter for single use — Jiangsu Suyun Medical Materials Co., Ltd. · Class IIa
- hi-slip plus — Wellspect HealthCare · Class I
- TruCath Oasis — H R Pharmaceuticals, Inc. · Class II
- SmoothCath™ — GELİŞİM MEDİKAL TIBBİ MALZ. PAZ. SAN. VE TİC. LTD. ŞTİ. · Class I
- PVC Hydrophilic Urethral Catheter — Chengdu Daxan Innovative Medical Tech. Co., Ltd. · Class II
- Sterile Urinary Catheter for single use — Jiangsu Suyun Medical Materials Co., Ltd. · Class IIa
- BeneCath® — Hangzhou Jimushi Meditech Co., Ltd. · Class II
- CompactCath Nelaton, Female, 14 Fr/Ch, 19cm — Lentismed d.o.o. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 610075D03P081S0258C4 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Hollister Incorporated
- EUDAMED SRN
- US-MF-000027818
- Authorised Representative
- Hollister ULC IE-AR-000022119
Sources (2)
- EUDAMED 3883a9c7-6c1e-4beb-8f57-fb9548f67cea 61 fields · synced Oct 6, 2026
- FDA UDI 06fcee09-26ec-4e84-8cf9-6409308e39e8 37 fields · synced May 30, 2026