GUDIDData
gudid Primary ID: FGS-0200

PillCam (UDI FGS-0200)

Manufactured by Covidien LP

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PillCam - Primary ID FGS-0200

Device Regulatory Overview

The PillCam (Model/Catalog Number: FGS-0200) is a medical device manufactured by Covidien LP. This product is indexed under FDA Product Code / Category Classification NEZ within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

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MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, IC Tray REF: 8888102004HP...

🔒 Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
FGS-0200
Product Code / EMDN
NEZ
Device Name
SB 2 capsule, 10-pack
Database Sync Date
2026-08-09 09:18:16

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 PillCam?

The registered manufacturer of record for PillCam is Covidien LP.

What is the Primary UDI-DI identifier for PillCam?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FGS-0200.

What classification code is assigned to this device?

This device is registered under product classification code NEZ.

Programmatic Export

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

JSON API Endpoint