gudid
Primary ID: CPF-KM 04 18-S
PERLA (UDI CPF-KM 04 18-S)
Manufactured by SpineArt SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PERLA - Primary ID CPF-KM 04 18-S
Device Regulatory Overview
The PERLA (Model/Catalog Number: CPF-KM 04 18-S) is a medical device manufactured by SpineArt SA. This product is indexed under FDA Product Code / Category Classification NKG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CPF-KM 04 18-S
- Product Code / EMDN
- NKG
- Device Name
- CANNULATED ML PREFERRED ANGLE SCREW
- Database Sync Date
- 2026-08-09 09:07:23
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 PERLA ?
The registered manufacturer of record for PERLA is SpineArt SA.
What is the Primary UDI-DI identifier for PERLA ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CPF-KM 04 18-S.
What classification code is assigned to this device?
This device is registered under product classification code NKG.
Similar Classification Devices (NKG)
Other Devices by SpineArt SA
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