eudamed_udi
Primary ID: *+D1060695222001*
Unspecified Brand (UDI *+D1060695222001*)
Manufactured by ABI Enterprises
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID *+D1060695222001*
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 06-9522-20) is a medical device manufactured by ABI Enterprises. This product is indexed under FDA Product Code / Category Classification L05090399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 06-9522-20
- Product Code / EMDN
- L05090399
- Device Name
- Teale Tenaculum Forceps
- Database Sync Date
- 2026-08-09 16:29:59
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is ABI Enterprises.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is *+D1060695222001*.
What classification code is assigned to this device?
This device is registered under product classification code L05090399.
Similar Classification Devices (L05090399)
Other Devices by ABI Enterprises
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