gudid
Primary ID: A20716A
Olympus (UDI A20716A)
Manufactured by OLYMPUS Winter & Ibe GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Olympus - Primary ID A20716A
Device Regulatory Overview
The Olympus (Model/Catalog Number: A20716A) is a medical device manufactured by OLYMPUS Winter & Ibe GmbH. This product is indexed under FDA Product Code / Category Classification KGE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A20716A
- Product Code / EMDN
- KGE
- Device Name
- Biopsy forceps, optical, unipolar, for 12 telescope
- Database Sync Date
- 2026-08-09 09:46:21
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 Olympus?
The registered manufacturer of record for Olympus is OLYMPUS Winter & Ibe GmbH.
What is the Primary UDI-DI identifier for Olympus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A20716A.
What classification code is assigned to this device?
This device is registered under product classification code KGE.
Similar Classification Devices (KGE)
Other Devices by OLYMPUS Winter & Ibe GmbH
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