PENTAX USYFITVUE GP1 L25G45B (UDI 04582428430981)
Manufactured by HOYA Technosurgical Corporation
Device Regulatory Overview
The PENTAX USYFITVUE GP1 L25G45B (Model/Catalog Number: 2037063) is a medical device manufactured by HOYA Technosurgical Corporation. This product is indexed under FDA Product Code / Category Classification L0316 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2037063
- Product Code / EMDN
- L0316
- Device Name
- PENTAX Surgical Loupes
- Database Sync Date
- 2026-08-09 16:29:00
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of PENTAX USYFITVUE GP1 L25G45B?
The registered manufacturer of record for PENTAX USYFITVUE GP1 L25G45B is HOYA Technosurgical Corporation.
What is the Primary UDI-DI identifier for PENTAX USYFITVUE GP1 L25G45B?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04582428430981.
What classification code is assigned to this device?
This device is registered under product classification code L0316.
Similar Classification Devices (L0316)
Other Devices by HOYA Technosurgical Corporation
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