Betica (UDI 06978111923393)
Manufactured by Promisemed Hangzhou Meditech Co., Ltd.
Device Regulatory Overview
The Betica (Model/Catalog Number: DPN-30*8) is a medical device manufactured by Promisemed Hangzhou Meditech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A0101010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DPN-30*8
- Product Code / EMDN
- A0101010201
- Device Name
- safety pen needle
- Database Sync Date
- 2026-08-09 16:50:37
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 Betica?
The registered manufacturer of record for Betica is Promisemed Hangzhou Meditech Co., Ltd..
What is the Primary UDI-DI identifier for Betica?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978111923393.
What classification code is assigned to this device?
This device is registered under product classification code A0101010201.
Similar Classification Devices (A0101010201)
Other Devices by Promisemed Hangzhou Meditech Co., Ltd.
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