Alleset (UDI 80-08159-HB)
Manufactured by GRI Medical & Electronic Technology Co., Ltd.
Device Regulatory Overview
The Alleset (Model/Catalog Number: 80-08159-HB) is a medical device manufactured by GRI Medical & Electronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification PUI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 80-08159-HB
- Product Code / EMDN
- PUI
- Device Name
- Ophthalmic Drape_Incise_W/Pouch_65X100IN_Non-Sterile_360ea/cs
- Database Sync Date
- 2026-08-09 09:00:28
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 Alleset?
The registered manufacturer of record for Alleset is GRI Medical & Electronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for Alleset?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 80-08159-HB.
What classification code is assigned to this device?
This device is registered under product classification code PUI.
Similar Classification Devices (PUI)
Other Devices by GRI Medical & Electronic Technology Co., Ltd.
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