eudamed_udi
Primary ID: 08052532971886
LETTINO BOTTICELLI PRO 4 SEG. PERLE (UDI 08052532971886)
Manufactured by FERROX srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LETTINO BOTTICELLI PRO 4 SEG. PERLE - Primary ID 08052532971886
Device Regulatory Overview
The LETTINO BOTTICELLI PRO 4 SEG. PERLE (Model/Catalog Number: 238001.9) is a medical device manufactured by FERROX srl. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 238001.9
- Product Code / EMDN
- Z12069099
- Device Name
- BOTTICELLI
- Database Sync Date
- 2026-08-09 16:29:02
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 LETTINO BOTTICELLI PRO 4 SEG. PERLE?
The registered manufacturer of record for LETTINO BOTTICELLI PRO 4 SEG. PERLE is FERROX srl.
What is the Primary UDI-DI identifier for LETTINO BOTTICELLI PRO 4 SEG. PERLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052532971886.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
Similar Classification Devices (Z12069099)
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