Operator (UDI 06947752813486)
Manufactured by Tianjin Bolang Science-Technology Development Co.,Ltd.
Device Regulatory Overview
The Operator (Model/Catalog Number: 111.242) is a medical device manufactured by Tianjin Bolang Science-Technology Development Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification Z12020707 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 111.242
- Product Code / EMDN
- Z12020707
- Device Name
- Resectoscopes
- Database Sync Date
- 2026-08-09 17:18:28
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 Operator?
The registered manufacturer of record for Operator is Tianjin Bolang Science-Technology Development Co.,Ltd..
What is the Primary UDI-DI identifier for Operator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06947752813486.
What classification code is assigned to this device?
This device is registered under product classification code Z12020707.
Similar Classification Devices (Z12020707)
Other Devices by Tianjin Bolang Science-Technology Development Co.,Ltd.
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