gudid
Primary ID: ERT PT
ERT PT (UDI ERT PT)
Manufactured by eResearchTechnology GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ERT PT - Primary ID ERT PT
Device Regulatory Overview
The ERT PT (Model/Catalog Number: ERT PT) is a medical device manufactured by eResearchTechnology GmbH. This product is indexed under FDA Product Code / Category Classification BTY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ERT PT
- Product Code / EMDN
- BTY
- Device Name
- Pneumotachograph tube, accessory, single-patient use
- Database Sync Date
- 2026-08-09 09:26:03
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 ERT PT?
The registered manufacturer of record for ERT PT is eResearchTechnology GmbH.
What is the Primary UDI-DI identifier for ERT PT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ERT PT.
What classification code is assigned to this device?
This device is registered under product classification code BTY.
Similar Classification Devices (BTY)
Other Devices by eResearchTechnology GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint