AS E.MOTION PRO (UDI 04046963769574)
Manufactured by Aesculap AG
Device Regulatory Overview
The AS E.MOTION PRO (Model/Catalog Number: NX625Z) is a medical device manufactured by Aesculap AG. This product is indexed under FDA Product Code / Category Classification P090908 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
- NX625Z
- Product Code / EMDN
- P090908
- Device Name
- E.MOTION augmentation implant
- Database Sync Date
- 2026-08-09 16:29:04
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 AS E.MOTION PRO?
The registered manufacturer of record for AS E.MOTION PRO is Aesculap AG.
What is the Primary UDI-DI identifier for AS E.MOTION PRO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046963769574.
What classification code is assigned to this device?
This device is registered under product classification code P090908.
Similar Classification Devices (P090908)
Other Devices by Aesculap AG
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