gudid
Primary ID: 05.1146.148
Monovette 1ml LH (UDI 05.1146.148)
Manufactured by Sarstedt Aktiengesellschaft & Co.KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Monovette 1ml LH - Primary ID 05.1146.148
Device Regulatory Overview
The Monovette 1ml LH (Model/Catalog Number: 05.1146.148) is a medical device manufactured by Sarstedt Aktiengesellschaft & Co.KG. This product is indexed under FDA Product Code / Category Classification JKA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 05.1146.148
- Product Code / EMDN
- JKA
- Device Name
- Database Sync Date
- 2026-08-09 09:11:41
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 Monovette 1ml LH?
The registered manufacturer of record for Monovette 1ml LH is Sarstedt Aktiengesellschaft & Co.KG.
What is the Primary UDI-DI identifier for Monovette 1ml LH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05.1146.148.
What classification code is assigned to this device?
This device is registered under product classification code JKA.
Similar Classification Devices (JKA)
Other Devices by Sarstedt Aktiengesellschaft & Co.KG
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