eudamed_udi
Primary ID: +E308199523820
21E (UDI +E308199523820)
Manufactured by W&H Sterilization Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 21E - Primary ID +E308199523820
Device Regulatory Overview
The 21E (Model/Catalog Number: 19952382) is a medical device manufactured by W&H Sterilization Srl. This product is indexed under FDA Product Code / Category Classification Z12011305 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 19952382
- Product Code / EMDN
- Z12011305
- Device Name
- 38671
- Database Sync Date
- 2026-08-09 17:06:49
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 21E?
The registered manufacturer of record for 21E is W&H Sterilization Srl.
What is the Primary UDI-DI identifier for 21E?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +E308199523820.
What classification code is assigned to this device?
This device is registered under product classification code Z12011305.
Similar Classification Devices (Z12011305)
Other Devices by W&H Sterilization Srl
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