Identity
- Trade Name
- LF FDA UDI
- Generic Name
- Urological operating table, electrohydraulic FDA UDI
- Device Name
- Drain Bag used with Hydra Vision or Direct Digital Urology Systems FDA UDI
- Model / Reference
- 335563 FDA UDI
- Description
- Drain Bag used with Hydra Vision or Direct Digital Urology Systems FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10746190002383 FDA UDI
- FDA Product Code
- KQS FDA UDI
- GMDN Term
- Urological operating table, electrohydraulic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.4890 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Lf by Liebel-Flarsheim Company, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 I | Pending data |
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Manufacturer
- Manufacturer
- Liebel-Flarsheim Company, LLC
Sources (1)
- FDA UDI 67ea0b30-9ae3-446f-8067-894b60e6c10b 34 fields · synced Jun 1, 2026