gudid
Primary ID: 4:1 Contra Angle with push-button latch head
Perfect Finish (UDI 4:1 Contra Angle with push-button latch head)
Manufactured by LARES RESEARCH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Perfect Finish - Primary ID 4:1 Contra Angle with push-button latch head
Device Regulatory Overview
The Perfect Finish (Model/Catalog Number: 4:1 Contra Angle with push-button latch head) is a medical device manufactured by LARES RESEARCH. This product is indexed under FDA Product Code / Category Classification EFB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4:1 Contra Angle with push-button latch head
- Product Code / EMDN
- EFB
- Device Name
- Perfect Finish 4:1 contra angle with push-button latch head
- Database Sync Date
- 2026-08-09 09:01:11
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 Perfect Finish?
The registered manufacturer of record for Perfect Finish is LARES RESEARCH.
What is the Primary UDI-DI identifier for Perfect Finish?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4:1 Contra Angle with push-button latch head.
What classification code is assigned to this device?
This device is registered under product classification code EFB.
Similar Classification Devices (EFB)
Other Devices by LARES RESEARCH
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