Sterile OBTURATOR for single use (Optical normal type) (UDI 05060911400288)
Manufactured by GENMED ENTERPRISES INTERNATIONAL LTD
Device Regulatory Overview
The Sterile OBTURATOR for single use (Optical normal type) (Model/Catalog Number: GN-TO1215-O) is a medical device manufactured by GENMED ENTERPRISES INTERNATIONAL LTD. This product is indexed under FDA Product Code / Category Classification K01010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GN-TO1215-O
- Product Code / EMDN
- K01010103
- Device Name
- Sterile Trocars for Single Use
- Database Sync Date
- 2026-08-09 16:48:34
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Sterile OBTURATOR for single use (Optical normal type)?
The registered manufacturer of record for Sterile OBTURATOR for single use (Optical normal type) is GENMED ENTERPRISES INTERNATIONAL LTD.
What is the Primary UDI-DI identifier for Sterile OBTURATOR for single use (Optical normal type)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060911400288.
What classification code is assigned to this device?
This device is registered under product classification code K01010103.
Similar Classification Devices (K01010103)
Other Devices by GENMED ENTERPRISES INTERNATIONAL LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint