eudamed_udi
Primary ID: 04262380371545
Z 32 HK (UDI 04262380371545)
Manufactured by Hermle Labortechnik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Z 32 HK - Primary ID 04262380371545
Device Regulatory Overview
The Z 32 HK (Model/Catalog Number: 311.00 V07) is a medical device manufactured by Hermle Labortechnik GmbH. This product is indexed under FDA Product Code / Category Classification W02069005 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 311.00 V07
- Product Code / EMDN
- W02069005
- Device Name
- Refrigerated Centrifuge
- Database Sync Date
- 2026-08-09 16:29:34
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 Z 32 HK?
The registered manufacturer of record for Z 32 HK is Hermle Labortechnik GmbH.
What is the Primary UDI-DI identifier for Z 32 HK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04262380371545.
What classification code is assigned to this device?
This device is registered under product classification code W02069005.
Similar Classification Devices (W02069005)
Other Devices by Hermle Labortechnik GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint