eudamed_udi
Primary ID: 06971254924951
LAPAROSCOPIC INSTRUMENT (UDI 06971254924951)
Manufactured by VHMED (Nantong) Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LAPAROSCOPIC INSTRUMENT - Primary ID 06971254924951
Device Regulatory Overview
The LAPAROSCOPIC INSTRUMENT (Model/Catalog Number: LS16028) is a medical device manufactured by VHMED (Nantong) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K01020104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LS16028
- Product Code / EMDN
- K01020104
- Device Name
- LAPAROSCOPIC INSTRUMENT
- Database Sync Date
- 2026-08-09 16:29:32
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of LAPAROSCOPIC INSTRUMENT?
The registered manufacturer of record for LAPAROSCOPIC INSTRUMENT is VHMED (Nantong) Co., Ltd..
What is the Primary UDI-DI identifier for LAPAROSCOPIC INSTRUMENT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971254924951.
What classification code is assigned to this device?
This device is registered under product classification code K01020104.
Similar Classification Devices (K01020104)
Other Devices by VHMED (Nantong) Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint