Identity
- Trade Name
- PLEUR-EVAC FDA UDI
- Generic Name
- General-purpose catheter connector, sterile FDA UDI
- Device Name
- PATIENT DRAINAGE TUBE LATEX FDA UDI
- Model / Reference
- IPN025426 FDA UDI
- Description
- PATIENT DRAINAGE TUBE LATEX FDA UDI
Identifiers
- Catalog Number
- S-1111 FDA UDI
- Primary DI / UDI-DI
- 34026704607342 FDA UDI
- FDA Product Code
- GAZ FDA UDI
- GMDN Term
- General-purpose catheter connector, sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Width — 1 Inch FDA UDILength — 15.5 Inch FDA UDI
Category: General-purpose catheter connector, sterile
Pleur-Evac by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General-purpose catheter connector, sterile.
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- Fluid Dock — Boston Scientific · Class II
- Custom Medical Specialties, Inc. — CUSTOM ASSEMBLIES, INC. · Class I
- Expel™ Large Capacity Drainage Catheter Connecting Tube — Boston Scientific · Class I
- AHD Luer Lock Cap — Argon Medical Devices, Inc. · Class II
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
- Teleflex Incorporated
Sources (1)
- FDA UDI 206fea8a-2a8f-4f39-af12-531003e63346 36 fields · synced Jun 1, 2026