gudid
Primary ID: QO.208.17
Quinelato (UDI QO.208.17)
Manufactured by Schobell Industrial Ltda
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Quinelato - Primary ID QO.208.17
Device Regulatory Overview
The Quinelato (Model/Catalog Number: QO.208.17) is a medical device manufactured by Schobell Industrial Ltda. This product is indexed under FDA Product Code / Category Classification FZT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- QO.208.17
- Product Code / EMDN
- FZT
- Device Name
- Ruskin Liston Bone Cutting Forceps 17cm Straight
- Database Sync Date
- 2026-08-09 09:07:19
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 Quinelato?
The registered manufacturer of record for Quinelato is Schobell Industrial Ltda.
What is the Primary UDI-DI identifier for Quinelato?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is QO.208.17.
What classification code is assigned to this device?
This device is registered under product classification code FZT.
Similar Classification Devices (FZT)
Other Devices by Schobell Industrial Ltda
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