Inflatable balloon (UDI 06931038600549)
Manufactured by Wenzhou Bokang Instruments Co.,Ltd
Device Regulatory Overview
The Inflatable balloon (Model/Catalog Number: E3 1103PM) is a medical device manufactured by Wenzhou Bokang Instruments Co.,Ltd. This product is indexed under FDA Product Code / Category Classification Z1203020299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E3 1103PM
- Product Code / EMDN
- Z1203020299
- Device Name
- Inflatable balloon
- Database Sync Date
- 2026-08-09 16:30:04
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 Inflatable balloon?
The registered manufacturer of record for Inflatable balloon is Wenzhou Bokang Instruments Co.,Ltd.
What is the Primary UDI-DI identifier for Inflatable balloon?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06931038600549.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020299.
Similar Classification Devices (Z1203020299)
Other Devices by Wenzhou Bokang Instruments Co.,Ltd
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