ACOFAR (UDI 16947872509280)
Manufactured by Shaoxing Gangfeng Hospital Products Co., Ltd.
Device Regulatory Overview
The ACOFAR (Model/Catalog Number: NMEB002) is a medical device manufactured by Shaoxing Gangfeng Hospital Products Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M0303010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NMEB002
- Product Code / EMDN
- M0303010203
- Device Name
- Medical elastic Bandege Poducts no sterile
- Database Sync Date
- 2026-08-09 16:46:38
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 ACOFAR?
The registered manufacturer of record for ACOFAR is Shaoxing Gangfeng Hospital Products Co., Ltd..
What is the Primary UDI-DI identifier for ACOFAR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16947872509280.
What classification code is assigned to this device?
This device is registered under product classification code M0303010203.
Similar Classification Devices (M0303010203)
Other Devices by Shaoxing Gangfeng Hospital Products Co., Ltd.
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