NEB 250 (UDI 06970229254949)
Manufactured by Globalcare Medical Technology Co., Ltd.
Device Regulatory Overview
The NEB 250 (Model/Catalog Number: p957300-3) is a medical device manufactured by Globalcare Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12159002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- p957300-3
- Product Code / EMDN
- Z12159002
- Device Name
- Aerosoltherapy Nebulizer
- Database Sync Date
- 2026-08-09 16:29:57
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 NEB 250?
The registered manufacturer of record for NEB 250 is Globalcare Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for NEB 250?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970229254949.
What classification code is assigned to this device?
This device is registered under product classification code Z12159002.
Similar Classification Devices (Z12159002)
Other Devices by Globalcare Medical Technology Co., Ltd.
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