eudamed_udi
Primary ID: 04712826092027
Rossmax (UDI 04712826092027)
Manufactured by Rossmax Innotek Corp.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rossmax - Primary ID 04712826092027
Device Regulatory Overview
The Rossmax (Model/Catalog Number: SB200) is a medical device manufactured by Rossmax Innotek Corp.. This product is indexed under FDA Product Code / Category Classification Z1203020408 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SB200
- Product Code / EMDN
- Z1203020408
- Device Name
- Fingertip Pulse Oximeter
- Database Sync Date
- 2026-08-09 16:28:50
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 Rossmax?
The registered manufacturer of record for Rossmax is Rossmax Innotek Corp..
What is the Primary UDI-DI identifier for Rossmax?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04712826092027.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020408.
Similar Classification Devices (Z1203020408)
Other Devices by Rossmax Innotek Corp.
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