CRANIOFIX ABSORBABLE (UDI FF017)
Manufactured by Aesculap AG
Device Regulatory Overview
The CRANIOFIX ABSORBABLE (Model/Catalog Number: FF017) is a medical device manufactured by Aesculap AG. This product is indexed under FDA Product Code / Category Classification GXR 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
- FF017
- Product Code / EMDN
- GXR
- Device Name
- 6 CRANIOFIX BURR HOLE CLAMP ABSORB.16MM
- Database Sync Date
- 2026-08-09 09:46:30
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 CRANIOFIX ABSORBABLE?
The registered manufacturer of record for CRANIOFIX ABSORBABLE is Aesculap AG.
What is the Primary UDI-DI identifier for CRANIOFIX ABSORBABLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FF017.
What classification code is assigned to this device?
This device is registered under product classification code GXR.
Similar Classification Devices (GXR)
Other Devices by Aesculap AG
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