gudid
Primary ID: 66054436
Pro Nozzle medium (UDI 66054436)
Manufactured by Heraeus Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pro Nozzle medium - Primary ID 66054436
Device Regulatory Overview
The Pro Nozzle medium (Model/Catalog Number: 66054436) is a medical device manufactured by Heraeus Medical GmbH. This product is indexed under FDA Product Code / Category Classification KIH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 66054436
- Product Code / EMDN
- KIH
- Device Name
- Nozzle to be used in combination with PALACOS Pro system
- Database Sync Date
- 2026-08-09 09:17:36
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 Pro Nozzle medium?
The registered manufacturer of record for Pro Nozzle medium is Heraeus Medical GmbH.
What is the Primary UDI-DI identifier for Pro Nozzle medium?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 66054436.
What classification code is assigned to this device?
This device is registered under product classification code KIH.
Similar Classification Devices (KIH)
Other Devices by Heraeus Medical GmbH
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