GUDIDData
eudamed_udi Primary ID: 07640156396942

WS-3 Sprague Rappaport Stethoscope (UDI 07640156396942)

Manufactured by B.Well Swiss AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WS-3 Sprague Rappaport Stethoscope - Primary ID 07640156396942

Device Regulatory Overview

The WS-3 Sprague Rappaport Stethoscope (Model/Catalog Number: 1101382) is a medical device manufactured by B.Well Swiss AG. This product is indexed under FDA Product Code / Category Classification C9005 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1101382
Product Code / EMDN
C9005
Device Name
Stethoscope
Database Sync Date
2026-08-09 16:51:02

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of WS-3 Sprague Rappaport Stethoscope?

The registered manufacturer of record for WS-3 Sprague Rappaport Stethoscope is B.Well Swiss AG.

What is the Primary UDI-DI identifier for WS-3 Sprague Rappaport Stethoscope?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640156396942.

What classification code is assigned to this device?

This device is registered under product classification code C9005.

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