eudamed_udi
Primary ID: 05051986000183
235mm Fine Toothed Forceps (UDI 05051986000183)
Manufactured by Surgical Innovations Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 235mm Fine Toothed Forceps - Primary ID 05051986000183
Device Regulatory Overview
The 235mm Fine Toothed Forceps (Model/Catalog Number: 101-47037) is a medical device manufactured by Surgical Innovations Ltd.. This product is indexed under FDA Product Code / Category Classification L180402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 101-47037
- Product Code / EMDN
- L180402
- Device Name
- 235mm Fine Toothed Forceps
- Database Sync Date
- 2026-08-09 16:51:56
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 235mm Fine Toothed Forceps?
The registered manufacturer of record for 235mm Fine Toothed Forceps is Surgical Innovations Ltd..
What is the Primary UDI-DI identifier for 235mm Fine Toothed Forceps?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051986000183.
What classification code is assigned to this device?
This device is registered under product classification code L180402.
Similar Classification Devices (L180402)
Other Devices by Surgical Innovations Ltd.
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