eudamed_udi
Primary ID: D-A.4021.1STCB
BLUSCOPE MIDI SELF-LIGHT (UDI D-A.4021.1STCB)
Manufactured by SAPI MED S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BLUSCOPE MIDI SELF-LIGHT - Primary ID D-A.4021.1STCB
Device Regulatory Overview
The BLUSCOPE MIDI SELF-LIGHT (Model/Catalog Number: A.4021.1ST) is a medical device manufactured by SAPI MED S.p.A.. This product is indexed under FDA Product Code / Category Classification G02060301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A.4021.1ST
- Product Code / EMDN
- G02060301
- Device Name
- Proctoscope
- Database Sync Date
- 2026-08-09 16:29:20
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 BLUSCOPE MIDI SELF-LIGHT?
The registered manufacturer of record for BLUSCOPE MIDI SELF-LIGHT is SAPI MED S.p.A..
What is the Primary UDI-DI identifier for BLUSCOPE MIDI SELF-LIGHT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-A.4021.1STCB.
What classification code is assigned to this device?
This device is registered under product classification code G02060301.
Similar Classification Devices (G02060301)
Other Devices by SAPI MED S.p.A.
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