gudid
Primary ID: 019.3117
P pro Try-In (UDI 019.3117)
Manufactured by DeltaMed GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for P pro Try-In - Primary ID 019.3117
Device Regulatory Overview
The P pro Try-In (Model/Catalog Number: 019.3117) is a medical device manufactured by DeltaMed GmbH. This product is indexed under FDA Product Code / Category Classification EEA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 019.3117
- Product Code / EMDN
- EEA
- Device Name
- P pro Try-In 1000g
- Database Sync Date
- 2026-08-09 09:53:17
Full Regulatory Attributes
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{
"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 pro Try-In?
The registered manufacturer of record for P pro Try-In is DeltaMed GmbH.
What is the Primary UDI-DI identifier for P pro Try-In?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 019.3117.
What classification code is assigned to this device?
This device is registered under product classification code EEA.
Similar Classification Devices (EEA)
Other Devices by DeltaMed GmbH
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