eudamed_udi
Primary ID: 05940540386712
LOWENSTEIN JENSEN + ISONIAZID 0.20 µg/mL (UDI 05940540386712)
Manufactured by DELTAROM SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LOWENSTEIN JENSEN + ISONIAZID 0.20 µg/mL - Primary ID 05940540386712
Device Regulatory Overview
The LOWENSTEIN JENSEN + ISONIAZID 0.20 µg/mL (Model/Catalog Number: 342947) is a medical device manufactured by DELTAROM SRL. This product is indexed under FDA Product Code / Category Classification W0104010206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 342947
- Product Code / EMDN
- W0104010206
- Device Name
- LOWENSTEIN JENSEN + ISONIAZID 0.20 µg/mL
- Database Sync Date
- 2026-08-09 16:28:52
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 LOWENSTEIN JENSEN + ISONIAZID 0.20 µg/mL?
The registered manufacturer of record for LOWENSTEIN JENSEN + ISONIAZID 0.20 µg/mL is DELTAROM SRL.
What is the Primary UDI-DI identifier for LOWENSTEIN JENSEN + ISONIAZID 0.20 µg/mL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940540386712.
What classification code is assigned to this device?
This device is registered under product classification code W0104010206.
Similar Classification Devices (W0104010206)
Other Devices by DELTAROM SRL
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