GUDIDData
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eudamed_udi Primary ID: 05055445965822

Recamier Uterine Curette Sharp - Rigid - Fig. 5 31 cm - 12 1/4" Width 12 mm Stainless Steel (UDI 05055445965822)

Manufactured by Surtex Instruments Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Recamier Uterine Curette Sharp - Rigid - Fig. 5 31 cm - 12 1/4" Width 12 mm Stainless Steel - Primary ID 05055445965822

Device Regulatory Overview

The Recamier Uterine Curette Sharp - Rigid - Fig. 5 31 cm - 12 1/4" Width 12 mm Stainless Steel (Model/Catalog Number: GY-710-12) is a medical device manufactured by Surtex Instruments Ltd. This product is indexed under FDA Product Code / Category Classification L050901 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
GY-710-12
Product Code / EMDN
L050901
Device Name
Cutting Instruments
Database Sync Date
2026-08-09 16:28:56

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Recamier Uterine Curette Sharp - Rigid - Fig. 5 31 cm - 12 1/4" Width 12 mm Stainless Steel?

The registered manufacturer of record for Recamier Uterine Curette Sharp - Rigid - Fig. 5 31 cm - 12 1/4" Width 12 mm Stainless Steel is Surtex Instruments Ltd.

What is the Primary UDI-DI identifier for Recamier Uterine Curette Sharp - Rigid - Fig. 5 31 cm - 12 1/4" Width 12 mm Stainless Steel?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05055445965822.

What classification code is assigned to this device?

This device is registered under product classification code L050901.

Similar Classification Devices (L050901)

Other Devices by Surtex Instruments Ltd

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