GUDIDData
eudamed_udi Primary ID: 03700569674533

Unspecified Brand (UDI 03700569674533)

Manufactured by Newclip Technics SAS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 03700569674533

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: ANC1680/B) is a medical device manufactured by Newclip Technics SAS. This product is indexed under FDA Product Code / Category Classification V0402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ANC1680/B
Product Code / EMDN
V0402
Device Name
Instrumentation class I
Database Sync Date
2026-08-09 16:28:58

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Newclip Technics SAS.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700569674533.

What classification code is assigned to this device?

This device is registered under product classification code V0402.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint