gudid Primary ID: FS-103

E+R (UDI FS-103)

Manufactured by Firstar Healthcare Company Limited (Guangzhou)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The E+R (Model/Catalog Number: FS-103) is a medical device manufactured by Firstar Healthcare Company Limited (Guangzhou). This product is indexed under FDA Product Code / Category Classification CBP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FS-103
Product Code / EMDN: CBP
Device Name
Database Sync Date: 2026-08-09 09:11:11

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 E+R?

The registered manufacturer of record for E+R is Firstar Healthcare Company Limited (Guangzhou).

What is the Primary UDI-DI identifier for E+R?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FS-103.

What classification code is assigned to this device?

This device is registered under product classification code CBP.

Similar Classification Devices (CBP)

Other Devices by Firstar Healthcare Company Limited (Guangzhou)

Programmatic Export

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

JSON API Endpoint