eudamed_udi
Primary ID: 00840095691161
Unspecified Brand (UDI 00840095691161)
Manufactured by Globe Scientific Europe B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 00840095691161
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 1402-10-200) is a medical device manufactured by Globe Scientific Europe B.V.. This product is indexed under FDA Product Code / Category Classification W0503900202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1402-10-200
- Product Code / EMDN
- W0503900202
- Device Name
- Cover Glass
- Database Sync Date
- 2026-08-09 16:29:32
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Globe Scientific Europe B.V..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840095691161.
What classification code is assigned to this device?
This device is registered under product classification code W0503900202.
Similar Classification Devices (W0503900202)
Other Devices by Globe Scientific Europe B.V.
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