gudid
Primary ID: P-Rohr Set SpiroPro
P-Rohr Set SpiroPro (UDI P-Rohr Set SpiroPro)
Manufactured by eResearchTechnology GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for P-Rohr Set SpiroPro - Primary ID P-Rohr Set SpiroPro
Device Regulatory Overview
The P-Rohr Set SpiroPro (Model/Catalog Number: P-Rohr Set SpiroPro) 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
- P-Rohr Set SpiroPro
- Product Code / EMDN
- BTY
- Device Name
- Set of ten Pneumotachograph tubes, single-patient use, accessory to SpiroPro
- 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
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of P-Rohr Set SpiroPro?
The registered manufacturer of record for P-Rohr Set SpiroPro is eResearchTechnology GmbH.
What is the Primary UDI-DI identifier for P-Rohr Set SpiroPro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P-Rohr Set SpiroPro.
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
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