eudamed_udi
Primary ID: 00628347568061
apotekets (UDI 00628347568061)
Manufactured by Artron Laboratories Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for apotekets - Primary ID 00628347568061
Device Regulatory Overview
The apotekets (Model/Catalog Number: A01-04-130AK2) is a medical device manufactured by Artron Laboratories Inc.. This product is indexed under FDA Product Code / Category Classification W0102160301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A01-04-130AK2
- Product Code / EMDN
- W0102160301
- Device Name
- Follicle Stimulating Hormone (FSH) Tests for self-testing
- Database Sync Date
- 2026-08-09 16:59:29
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 apotekets?
The registered manufacturer of record for apotekets is Artron Laboratories Inc..
What is the Primary UDI-DI identifier for apotekets?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00628347568061.
What classification code is assigned to this device?
This device is registered under product classification code W0102160301.
Similar Classification Devices (W0102160301)
Other Devices by Artron Laboratories Inc.
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