ERGOPLANT (UDI 04046963322229)
Manufactured by Aesculap AG
Device Regulatory Overview
The ERGOPLANT (Model/Catalog Number: DX506T) is a medical device manufactured by Aesculap AG. This product is indexed under FDA Product Code / Category Classification L150201 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R....
AESCULAP ELAN 4 FIXED DURAGUARD LONG. Model Number: GB943R....
Technical Specifications
- Model Number
- DX506T
- Product Code / EMDN
- L150201
- Device Name
- Bone Split instrument dental
- Database Sync Date
- 2026-08-09 16:45:45
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 ERGOPLANT?
The registered manufacturer of record for ERGOPLANT is Aesculap AG.
What is the Primary UDI-DI identifier for ERGOPLANT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046963322229.
What classification code is assigned to this device?
This device is registered under product classification code L150201.
Similar Classification Devices (L150201)
Other Devices by Aesculap AG
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