Identity
- Trade Name
- LG-150-CNN-PL FDA UDI
- Generic Name
- Urogenital surgical laser system beam guide, single-use FDA UDI
- Device Name
- LaseGuide™ Connect Nav 150u Laser Fiber PL FDA UDI
- Model / Reference
- LG-150-CNN-PL FDA UDI
- Description
- LaseGuide™ Connect Nav 150u Laser Fiber PL FDA UDI
Identifiers
- Catalog Number
- LG-150-CNN-PL FDA UDI
- Primary DI / UDI-DI
- 00816469021049 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- Urogenital surgical laser system beam guide, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Urogenital surgical laser system beam guide, single-use
Lg-150-Cnn-Pl by Laser Peripherals Llc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Urogenital surgical laser system beam guide, single-use.
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- LEONI™ — WEINERT Fiber Optics Inc. · Class II
- Cook — COOK INCORPORATED · Class II
- Laser Engineering — LASER ENGINEERING, INC. · Class II
- Surgimedics® — COASTAL LIFE TECHNOLOGIES, INC. · Class II
- LEONI™ — WEINERT Fiber Optics 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
- Laser Peripherals Llc.
Sources (1)
- FDA UDI 3c67392c-c000-4210-98e1-12c16295524b 34 fields · synced May 30, 2026