gudid
Primary ID: 34-15
Ultradrape (UDI 34-15)
Manufactured by PARKER LABORATORIES INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ultradrape - Primary ID 34-15
Device Regulatory Overview
The Ultradrape (Model/Catalog Number: 34-15) is a medical device manufactured by PARKER LABORATORIES INC. This product is indexed under FDA Product Code / Category Classification GYB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 34-15
- Product Code / EMDN
- GYB
- Device Name
- Ultrasound Guided Peripheral Intravenous Barrier and Securement Device 3.25''x5.8''
- Database Sync Date
- 2026-08-09 09:58:58
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 Ultradrape?
The registered manufacturer of record for Ultradrape is PARKER LABORATORIES INC.
What is the Primary UDI-DI identifier for Ultradrape?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 34-15.
What classification code is assigned to this device?
This device is registered under product classification code GYB.
Similar Classification Devices (GYB)
Other Devices by PARKER LABORATORIES INC
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