gudid
Primary ID: WB990211
Olympus (UDI WB990211)
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 WB990211
Device Regulatory Overview
The Olympus (Model/Catalog Number: WB990211) is a medical device manufactured by OLYMPUS Winter & Ibe GmbH. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WB990211
- Product Code / EMDN
- GEI
- Device Name
- Database Sync Date
- 2026-08-09 09:29:23
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 WB990211.
What classification code is assigned to this device?
This device is registered under product classification code GEI.
Similar Classification Devices (GEI)
Other Devices by OLYMPUS Winter & Ibe GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint