Burette Infusion Set (UDI 06971956737767)
Manufactured by Ningbo MFLAB Medical Instruments Co., Ltd.
Device Regulatory Overview
The Burette Infusion Set (Model/Catalog Number: 124.15) is a medical device manufactured by Ningbo MFLAB Medical Instruments Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A03010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 124.15
- Product Code / EMDN
- A03010199
- Device Name
- Burette Infusion Set
- Database Sync Date
- 2026-08-09 16:29:02
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 Burette Infusion Set?
The registered manufacturer of record for Burette Infusion Set is Ningbo MFLAB Medical Instruments Co., Ltd..
What is the Primary UDI-DI identifier for Burette Infusion Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971956737767.
What classification code is assigned to this device?
This device is registered under product classification code A03010199.
Similar Classification Devices (A03010199)
Other Devices by Ningbo MFLAB Medical Instruments Co., Ltd.
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