Bio Miratray OK, S2, 50er (UDI 04099637006116)
Manufactured by Hager & Werken GmbH & Co. KG
Device Regulatory Overview
The Bio Miratray OK, S2, 50er (Model/Catalog Number: 641141) is a medical device manufactured by Hager & Werken GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Q010503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 641141
- Product Code / EMDN
- Q010503
- Device Name
- Abformlöffel, einmalige Anwendung
- Database Sync Date
- 2026-08-09 16:28:49
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 Bio Miratray OK, S2, 50er?
The registered manufacturer of record for Bio Miratray OK, S2, 50er is Hager & Werken GmbH & Co. KG.
What is the Primary UDI-DI identifier for Bio Miratray OK, S2, 50er?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04099637006116.
What classification code is assigned to this device?
This device is registered under product classification code Q010503.
Similar Classification Devices (Q010503)
Other Devices by Hager & Werken GmbH & Co. KG
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