Identity
- Trade Name
- LSO QuickSet FDA UDI
- Generic Name
- Ophthalmic irrigation/infusion/aspiration tubing, single-use FDA UDI
- Device Name
- A device adapter that connects VFI machines to a syringe, providing pressurized air in assisting clinicians in depressing syringe. FDA UDI
- Model / Reference
- LQ2000 FDA UDI
- Description
- A device adapter that connects VFI machines to a syringe, providing pressurized air in assisting clinicians in depressing syringe. FDA UDI
Identifiers
- Catalog Number
- N/A FDA UDI
- Primary DI / UDI-DI
- 00871321002215 FDA UDI
- FDA Product Code
- IQG FDA UDI
- GMDN Term
- Ophthalmic irrigation/infusion/aspiration tubing, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 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
Yes
FDA UDI
Category: Ophthalmic irrigation/infusion/aspiration tubing, single-use
LSO QuickSet by Labtician Ophthalmics, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Labtician Ophthalmics, Inc
Sources (1)
- FDA UDI cd108d8f-7799-446c-a2b4-f94e40cfe8de 35 fields · synced May 30, 2026