eudamed_udi
Primary ID: 07613365000139
BP-200 plus (Base device SpO2) (UDI 07613365000139)
Manufactured by SCHILLER AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BP-200 plus (Base device SpO2) - Primary ID 07613365000139
Device Regulatory Overview
The BP-200 plus (Base device SpO2) (Model/Catalog Number: 3.930301) is a medical device manufactured by SCHILLER AG. This product is indexed under FDA Product Code / Category Classification Z1203020302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3.930301
- Product Code / EMDN
- Z1203020302
- Device Name
- BP-200 plus (Base device SpO2)
- Database Sync Date
- 2026-08-09 16:51:17
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 BP-200 plus (Base device SpO2)?
The registered manufacturer of record for BP-200 plus (Base device SpO2) is SCHILLER AG.
What is the Primary UDI-DI identifier for BP-200 plus (Base device SpO2)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613365000139.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020302.
Similar Classification Devices (Z1203020302)
Other Devices by SCHILLER AG
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