eudamed_udi
Primary ID: 42514018038680
Retractor The Mild Nr. 2 (UDI 42514018038680)
Manufactured by endocon GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Retractor The Mild Nr. 2 - Primary ID 42514018038680
Device Regulatory Overview
The Retractor The Mild Nr. 2 (Model/Catalog Number: 9100063 endocon catalogue) is a medical device manufactured by endocon GmbH. This product is indexed under FDA Product Code / Category Classification L0915 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9100063 endocon catalogue
- Product Code / EMDN
- L0915
- Device Name
- Revisionsinstrumentensystem
- Database Sync Date
- 2026-08-09 16:29:55
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 Retractor The Mild Nr. 2?
The registered manufacturer of record for Retractor The Mild Nr. 2 is endocon GmbH.
What is the Primary UDI-DI identifier for Retractor The Mild Nr. 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 42514018038680.
What classification code is assigned to this device?
This device is registered under product classification code L0915.
Similar Classification Devices (L0915)
Other Devices by endocon GmbH
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