GUDIDData
gudid Primary ID: 20325-211

ERBEFLO 2 (UDI 20325-211)

Manufactured by Erbe Medical, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ERBEFLO 2 - Primary ID 20325-211

Device Regulatory Overview

The ERBEFLO 2 (Model/Catalog Number: 20325-211) is a medical device manufactured by Erbe Medical, LLC. This product is indexed under FDA Product Code / Category Classification OCX 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.

ID: Z-2062-2026 View Full Alert →

ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2 Tubing/Cap Set for Olympus Sco...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-2063-2026 View Full Alert →

ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes, 20325-201; ERBEFLO CleverCap Hybrid Tubing/Cap Set for Fujifilm Scopes, REF: 20...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-2064-2026 View Full Alert →

ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222...

🔒 Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
20325-211
Product Code / EMDN
OCX
Device Name
Endoscopy Port Connector for Olympus Scopes
Database Sync Date
2026-08-09 09:11:42

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 ERBEFLO 2?

The registered manufacturer of record for ERBEFLO 2 is Erbe Medical, LLC.

What is the Primary UDI-DI identifier for ERBEFLO 2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20325-211.

What classification code is assigned to this device?

This device is registered under product classification code OCX.

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