Identity
- Trade Name
- Universal Y Connector FDA UDI
- Generic Name
- Closed-wound drain connector FDA UDI
- Device Name
- Universal Y Connector FDA UDI
- Model / Reference
- WD-20 FDA UDI
- Description
- Universal Y Connector FDA UDI
Identifiers
- Primary DI / UDI-DI
- B040WD201 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- Closed-wound drain connector 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Closed-wound drain connector
Universal Y Connector by Genesee Biomedical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Closed-wound drain connector.
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- Custom Medical Specialties, Inc. — CUSTOM ASSEMBLIES, INC. · Class I
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- Hemovac® Wound Drainage System — Zimmer Orthopaedic Surgical Products · Class I
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
- Genesee Biomedical, Inc.
Sources (1)
- FDA UDI ff971703-9321-4d7c-b9ea-e49a88116e37 34 fields · synced May 30, 2026