DORNHOFFER ALTO PARTIAL (UDI 695)
Manufactured by Grace Medical, Inc.
Device Regulatory Overview
The DORNHOFFER ALTO PARTIAL (Model/Catalog Number: 695) is a medical device manufactured by Grace Medical, Inc.. This product is indexed under FDA Product Code / Category Classification ETB within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis...
Technical Specifications
- Model Number
- 695
- Product Code / EMDN
- ETB
- Device Name
- DORNHOFFER ALTO PARTIAL SIZERS INCLUDED HA/TITANIUM/SILICONE
- Database Sync Date
- 2026-08-09 09:59:39
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 DORNHOFFER ALTO PARTIAL?
The registered manufacturer of record for DORNHOFFER ALTO PARTIAL is Grace Medical, Inc..
What is the Primary UDI-DI identifier for DORNHOFFER ALTO PARTIAL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 695.
What classification code is assigned to this device?
This device is registered under product classification code ETB.
Similar Classification Devices (ETB)
Other Devices by Grace Medical, Inc.
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