eudamed_udi
Primary ID: 04711605994460
Veress Needle (UDI 04711605994460)
Manufactured by Advanced Medical Design Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Veress Needle - Primary ID 04711605994460
Device Regulatory Overview
The Veress Needle (Model/Catalog Number: AVN-S150) is a medical device manufactured by Advanced Medical Design Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K0104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AVN-S150
- Product Code / EMDN
- K0104
- Device Name
- Veress Needle
- Database Sync Date
- 2026-08-09 16:59:28
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 Veress Needle?
The registered manufacturer of record for Veress Needle is Advanced Medical Design Co., Ltd..
What is the Primary UDI-DI identifier for Veress Needle?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04711605994460.
What classification code is assigned to this device?
This device is registered under product classification code K0104.
Similar Classification Devices (K0104)
Other Devices by Advanced Medical Design Co., Ltd.
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