eudamed_udi
Primary ID: 08059224185682
STELO INSERITORE SEEGER (UDI 08059224185682)
Manufactured by Rhein 83 S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STELO INSERITORE SEEGER - Primary ID 08059224185682
Device Regulatory Overview
The STELO INSERITORE SEEGER (Model/Catalog Number: 190IS) is a medical device manufactured by Rhein 83 S.r.l.. This product is indexed under FDA Product Code / Category Classification Q010280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 190IS
- Product Code / EMDN
- Q010280
- Device Name
- Strumenti (Regola 1)
- Database Sync Date
- 2026-08-09 16:28:47
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 STELO INSERITORE SEEGER?
The registered manufacturer of record for STELO INSERITORE SEEGER is Rhein 83 S.r.l..
What is the Primary UDI-DI identifier for STELO INSERITORE SEEGER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08059224185682.
What classification code is assigned to this device?
This device is registered under product classification code Q010280.
Similar Classification Devices (Q010280)
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