ERBEFLO 2 (UDI 20325-211)
Manufactured by Erbe Medical, LLC
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.
Enforcement actions are currently active for this product line.
ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2 Tubing/Cap Set for Olympus Sco...
ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes, 20325-201; ERBEFLO CleverCap Hybrid Tubing/Cap Set for Fujifilm Scopes, REF: 20...
ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222...
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
}
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 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.
Similar Classification Devices (OCX)
Other Devices by Erbe Medical, LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint