Identity
- Trade Name
- Steris FDA UDI
- Generic Name
- Urological fluid funnel FDA UDI
- Device Name
- Urology Drain Bag FDA UDI
- Model / Reference
- 31780 N/S FDA UDI
- Description
- Urology Drain Bag FDA UDI
Identifiers
- Catalog Number
- BF459 (056404-709) FDA UDI
- Primary DI / UDI-DI
- 00618125192274 FDA UDI
- FDA Product Code
- MMZ FDA UDI
- GMDN Term
- Urological fluid funnel FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4890 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Urological fluid funnel
Steris by Tidi Products, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Uro drain tray — Skytron, LLC · Class I
- Sterimed — Sterimed, Inc. · 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
- Tidi Products, Llc
Sources (1)
- FDA UDI 12921e66-3e47-4a39-b37b-46583d69ee08 34 fields · synced May 30, 2026