eudamed_udi
Primary ID: 05055860849974
901B (UDI 05055860849974)
Manufactured by Sunoptic International Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 901B - Primary ID 05055860849974
Device Regulatory Overview
The 901B (Model/Catalog Number: 901B) is a medical device manufactured by Sunoptic International Ltd. This product is indexed under FDA Product Code / Category Classification Q02100201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 901B
- Product Code / EMDN
- Q02100201
- Device Name
- Frames Metal Mix
- Database Sync Date
- 2026-08-09 16:28:51
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 901B?
The registered manufacturer of record for 901B is Sunoptic International Ltd.
What is the Primary UDI-DI identifier for 901B?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05055860849974.
What classification code is assigned to this device?
This device is registered under product classification code Q02100201.
Similar Classification Devices (Q02100201)
Other Devices by Sunoptic International Ltd
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