eudamed_udi
Primary ID: 04066625001255
INTERMED Schnelldesinfektion N (UDI 04066625001255)
Manufactured by bioSight GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INTERMED Schnelldesinfektion N - Primary ID 04066625001255
Device Regulatory Overview
The INTERMED Schnelldesinfektion N (Model/Catalog Number: 211927) is a medical device manufactured by bioSight GmbH. This product is indexed under FDA Product Code / Category Classification D0701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 211927
- Product Code / EMDN
- D0701
- Device Name
- N.A.
- 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 INTERMED Schnelldesinfektion N?
The registered manufacturer of record for INTERMED Schnelldesinfektion N is bioSight GmbH.
What is the Primary UDI-DI identifier for INTERMED Schnelldesinfektion N?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04066625001255.
What classification code is assigned to this device?
This device is registered under product classification code D0701.
Similar Classification Devices (D0701)
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