gudid
Primary ID: QS.852.03
Schobell (UDI QS.852.03)
Manufactured by Schobell Industrial Ltda
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Schobell - Primary ID QS.852.03
Device Regulatory Overview
The Schobell (Model/Catalog Number: QS.852.03) is a medical device manufactured by Schobell Industrial Ltda. This product is indexed under FDA Product Code / Category Classification HDQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- QS.852.03
- Product Code / EMDN
- HDQ
- Device Name
- Gaylor Prof. Medina Biopsy forceps 2mm
- Database Sync Date
- 2026-08-09 09:07:14
Full Regulatory Attributes
🔒 Token Gated
{
"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 Schobell?
The registered manufacturer of record for Schobell is Schobell Industrial Ltda.
What is the Primary UDI-DI identifier for Schobell?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is QS.852.03.
What classification code is assigned to this device?
This device is registered under product classification code HDQ.
Similar Classification Devices (HDQ)
Other Devices by Schobell Industrial Ltda
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