eudamed_udi
Primary ID: +E308190100040
seethroughFLEX XRE-200 (UDI +E308190100040)
Manufactured by W&H Sterilization Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for seethroughFLEX XRE-200 - Primary ID +E308190100040
Device Regulatory Overview
The seethroughFLEX XRE-200 (Model/Catalog Number: 19010004) is a medical device manufactured by W&H Sterilization Srl. This product is indexed under FDA Product Code / Category Classification Z1103030102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 19010004
- Product Code / EMDN
- Z1103030102
- Device Name
- 61019
- Database Sync Date
- 2026-08-09 17:16:44
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 seethroughFLEX XRE-200?
The registered manufacturer of record for seethroughFLEX XRE-200 is W&H Sterilization Srl.
What is the Primary UDI-DI identifier for seethroughFLEX XRE-200?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +E308190100040.
What classification code is assigned to this device?
This device is registered under product classification code Z1103030102.
Similar Classification Devices (Z1103030102)
Other Devices by W&H Sterilization Srl
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